Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges
Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have e...
Ausführliche Beschreibung
Autor*in: |
Tanić, Miljana [verfasserIn] |
---|
Format: |
E-Artikel |
---|---|
Sprache: |
Englisch |
Erschienen: |
2017transfer abstract |
---|
Umfang: |
8 |
---|
Übergeordnetes Werk: |
Enthalten in: Hybrid carbon fiber composite lattice truss structures - George, T. ELSEVIER, 2014transfer abstract, reviews of all advances : evaluation of key references : comprehensive listing of papers, Amsterdam |
---|---|
Übergeordnetes Werk: |
volume:42 ; year:2017 ; pages:48-55 ; extent:8 |
Links: |
---|
DOI / URN: |
10.1016/j.gde.2017.01.017 |
---|
Katalog-ID: |
ELV040524299 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | ELV040524299 | ||
003 | DE-627 | ||
005 | 20230625232106.0 | ||
007 | cr uuu---uuuuu | ||
008 | 180603s2017 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.gde.2017.01.017 |2 doi | |
028 | 5 | 2 | |a GBVA2017016000012.pica |
035 | |a (DE-627)ELV040524299 | ||
035 | |a (ELSEVIER)S0959-437X(17)30018-7 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
082 | 0 | |a 610 | |
082 | 0 | 4 | |a 610 |q DE-600 |
082 | 0 | 4 | |a 660 |q VZ |
082 | 0 | 4 | |a 610 |q VZ |
082 | 0 | 4 | |a 580 |a 540 |q VZ |
084 | |a BIODIV |q DE-30 |2 fid | ||
084 | |a 42.00 |2 bkl | ||
100 | 1 | |a Tanić, Miljana |e verfasserin |4 aut | |
245 | 1 | 0 | |a Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges |
264 | 1 | |c 2017transfer abstract | |
300 | |a 8 | ||
336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
337 | |a nicht spezifiziert |b z |2 rdamedia | ||
338 | |a nicht spezifiziert |b zu |2 rdacarrier | ||
520 | |a Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. | ||
520 | |a Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. | ||
700 | 1 | |a Beck, Stephan |4 oth | |
773 | 0 | 8 | |i Enthalten in |n Elsevier |a George, T. ELSEVIER |t Hybrid carbon fiber composite lattice truss structures |d 2014transfer abstract |d reviews of all advances : evaluation of key references : comprehensive listing of papers |g Amsterdam |w (DE-627)ELV022997628 |
773 | 1 | 8 | |g volume:42 |g year:2017 |g pages:48-55 |g extent:8 |
856 | 4 | 0 | |u https://doi.org/10.1016/j.gde.2017.01.017 |3 Volltext |
912 | |a GBV_USEFLAG_U | ||
912 | |a GBV_ELV | ||
912 | |a SYSFLAG_U | ||
912 | |a FID-BIODIV | ||
912 | |a SSG-OLC-PHA | ||
912 | |a GBV_ILN_73 | ||
936 | b | k | |a 42.00 |j Biologie: Allgemeines |q VZ |
951 | |a AR | ||
952 | |d 42 |j 2017 |h 48-55 |g 8 | ||
953 | |2 045F |a 610 |
author_variant |
m t mt |
---|---|
matchkey_str |
tanimiljanabeckstephan:2017----:pgnmwdascaintdefracrimredsoeynicltnclfedae |
hierarchy_sort_str |
2017transfer abstract |
bklnumber |
42.00 |
publishDate |
2017 |
allfields |
10.1016/j.gde.2017.01.017 doi GBVA2017016000012.pica (DE-627)ELV040524299 (ELSEVIER)S0959-437X(17)30018-7 DE-627 ger DE-627 rakwb eng 610 610 DE-600 660 VZ 610 VZ 580 540 VZ BIODIV DE-30 fid 42.00 bkl Tanić, Miljana verfasserin aut Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges 2017transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Beck, Stephan oth Enthalten in Elsevier George, T. ELSEVIER Hybrid carbon fiber composite lattice truss structures 2014transfer abstract reviews of all advances : evaluation of key references : comprehensive listing of papers Amsterdam (DE-627)ELV022997628 volume:42 year:2017 pages:48-55 extent:8 https://doi.org/10.1016/j.gde.2017.01.017 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA GBV_ILN_73 42.00 Biologie: Allgemeines VZ AR 42 2017 48-55 8 045F 610 |
spelling |
10.1016/j.gde.2017.01.017 doi GBVA2017016000012.pica (DE-627)ELV040524299 (ELSEVIER)S0959-437X(17)30018-7 DE-627 ger DE-627 rakwb eng 610 610 DE-600 660 VZ 610 VZ 580 540 VZ BIODIV DE-30 fid 42.00 bkl Tanić, Miljana verfasserin aut Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges 2017transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Beck, Stephan oth Enthalten in Elsevier George, T. ELSEVIER Hybrid carbon fiber composite lattice truss structures 2014transfer abstract reviews of all advances : evaluation of key references : comprehensive listing of papers Amsterdam (DE-627)ELV022997628 volume:42 year:2017 pages:48-55 extent:8 https://doi.org/10.1016/j.gde.2017.01.017 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA GBV_ILN_73 42.00 Biologie: Allgemeines VZ AR 42 2017 48-55 8 045F 610 |
allfields_unstemmed |
10.1016/j.gde.2017.01.017 doi GBVA2017016000012.pica (DE-627)ELV040524299 (ELSEVIER)S0959-437X(17)30018-7 DE-627 ger DE-627 rakwb eng 610 610 DE-600 660 VZ 610 VZ 580 540 VZ BIODIV DE-30 fid 42.00 bkl Tanić, Miljana verfasserin aut Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges 2017transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Beck, Stephan oth Enthalten in Elsevier George, T. ELSEVIER Hybrid carbon fiber composite lattice truss structures 2014transfer abstract reviews of all advances : evaluation of key references : comprehensive listing of papers Amsterdam (DE-627)ELV022997628 volume:42 year:2017 pages:48-55 extent:8 https://doi.org/10.1016/j.gde.2017.01.017 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA GBV_ILN_73 42.00 Biologie: Allgemeines VZ AR 42 2017 48-55 8 045F 610 |
allfieldsGer |
10.1016/j.gde.2017.01.017 doi GBVA2017016000012.pica (DE-627)ELV040524299 (ELSEVIER)S0959-437X(17)30018-7 DE-627 ger DE-627 rakwb eng 610 610 DE-600 660 VZ 610 VZ 580 540 VZ BIODIV DE-30 fid 42.00 bkl Tanić, Miljana verfasserin aut Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges 2017transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Beck, Stephan oth Enthalten in Elsevier George, T. ELSEVIER Hybrid carbon fiber composite lattice truss structures 2014transfer abstract reviews of all advances : evaluation of key references : comprehensive listing of papers Amsterdam (DE-627)ELV022997628 volume:42 year:2017 pages:48-55 extent:8 https://doi.org/10.1016/j.gde.2017.01.017 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA GBV_ILN_73 42.00 Biologie: Allgemeines VZ AR 42 2017 48-55 8 045F 610 |
allfieldsSound |
10.1016/j.gde.2017.01.017 doi GBVA2017016000012.pica (DE-627)ELV040524299 (ELSEVIER)S0959-437X(17)30018-7 DE-627 ger DE-627 rakwb eng 610 610 DE-600 660 VZ 610 VZ 580 540 VZ BIODIV DE-30 fid 42.00 bkl Tanić, Miljana verfasserin aut Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges 2017transfer abstract 8 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. Beck, Stephan oth Enthalten in Elsevier George, T. ELSEVIER Hybrid carbon fiber composite lattice truss structures 2014transfer abstract reviews of all advances : evaluation of key references : comprehensive listing of papers Amsterdam (DE-627)ELV022997628 volume:42 year:2017 pages:48-55 extent:8 https://doi.org/10.1016/j.gde.2017.01.017 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA GBV_ILN_73 42.00 Biologie: Allgemeines VZ AR 42 2017 48-55 8 045F 610 |
language |
English |
source |
Enthalten in Hybrid carbon fiber composite lattice truss structures Amsterdam volume:42 year:2017 pages:48-55 extent:8 |
sourceStr |
Enthalten in Hybrid carbon fiber composite lattice truss structures Amsterdam volume:42 year:2017 pages:48-55 extent:8 |
format_phy_str_mv |
Article |
bklname |
Biologie: Allgemeines |
institution |
findex.gbv.de |
dewey-raw |
610 |
isfreeaccess_bool |
false |
container_title |
Hybrid carbon fiber composite lattice truss structures |
authorswithroles_txt_mv |
Tanić, Miljana @@aut@@ Beck, Stephan @@oth@@ |
publishDateDaySort_date |
2017-01-01T00:00:00Z |
hierarchy_top_id |
ELV022997628 |
dewey-sort |
3610 |
id |
ELV040524299 |
language_de |
englisch |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV040524299</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230625232106.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2017 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.gde.2017.01.017</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2017016000012.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV040524299</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0959-437X(17)30018-7</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">610</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">660</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">580</subfield><subfield code="a">540</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">BIODIV</subfield><subfield code="q">DE-30</subfield><subfield code="2">fid</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">42.00</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Tanić, Miljana</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2017transfer abstract</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">8</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Beck, Stephan</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier</subfield><subfield code="a">George, T. ELSEVIER</subfield><subfield code="t">Hybrid carbon fiber composite lattice truss structures</subfield><subfield code="d">2014transfer abstract</subfield><subfield code="d">reviews of all advances : evaluation of key references : comprehensive listing of papers</subfield><subfield code="g">Amsterdam</subfield><subfield code="w">(DE-627)ELV022997628</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:42</subfield><subfield code="g">year:2017</subfield><subfield code="g">pages:48-55</subfield><subfield code="g">extent:8</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.gde.2017.01.017</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">FID-BIODIV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">42.00</subfield><subfield code="j">Biologie: Allgemeines</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">42</subfield><subfield code="j">2017</subfield><subfield code="h">48-55</subfield><subfield code="g">8</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">610</subfield></datafield></record></collection>
|
author |
Tanić, Miljana |
spellingShingle |
Tanić, Miljana ddc 610 ddc 660 ddc 580 fid BIODIV bkl 42.00 Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges |
authorStr |
Tanić, Miljana |
ppnlink_with_tag_str_mv |
@@773@@(DE-627)ELV022997628 |
format |
electronic Article |
dewey-ones |
610 - Medicine & health 660 - Chemical engineering 580 - Plants (Botany) 540 - Chemistry & allied sciences |
delete_txt_mv |
keep |
author_role |
aut |
collection |
elsevier |
remote_str |
true |
illustrated |
Not Illustrated |
topic_title |
610 610 DE-600 660 VZ 610 VZ 580 540 VZ BIODIV DE-30 fid 42.00 bkl Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges |
topic |
ddc 610 ddc 660 ddc 580 fid BIODIV bkl 42.00 |
topic_unstemmed |
ddc 610 ddc 660 ddc 580 fid BIODIV bkl 42.00 |
topic_browse |
ddc 610 ddc 660 ddc 580 fid BIODIV bkl 42.00 |
format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
format_main_str_mv |
Text Zeitschrift/Artikel |
carriertype_str_mv |
zu |
author2_variant |
s b sb |
hierarchy_parent_title |
Hybrid carbon fiber composite lattice truss structures |
hierarchy_parent_id |
ELV022997628 |
dewey-tens |
610 - Medicine & health 660 - Chemical engineering 580 - Plants (Botany) 540 - Chemistry |
hierarchy_top_title |
Hybrid carbon fiber composite lattice truss structures |
isfreeaccess_txt |
false |
familylinks_str_mv |
(DE-627)ELV022997628 |
title |
Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges |
ctrlnum |
(DE-627)ELV040524299 (ELSEVIER)S0959-437X(17)30018-7 |
title_full |
Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges |
author_sort |
Tanić, Miljana |
journal |
Hybrid carbon fiber composite lattice truss structures |
journalStr |
Hybrid carbon fiber composite lattice truss structures |
lang_code |
eng |
isOA_bool |
false |
dewey-hundreds |
600 - Technology 500 - Science |
recordtype |
marc |
publishDateSort |
2017 |
contenttype_str_mv |
zzz |
container_start_page |
48 |
author_browse |
Tanić, Miljana |
container_volume |
42 |
physical |
8 |
class |
610 610 DE-600 660 VZ 610 VZ 580 540 VZ BIODIV DE-30 fid 42.00 bkl |
format_se |
Elektronische Aufsätze |
author-letter |
Tanić, Miljana |
doi_str_mv |
10.1016/j.gde.2017.01.017 |
dewey-full |
610 660 580 540 |
title_sort |
epigenome-wide association studies for cancer biomarker discovery in circulating cell-free dna: technical advances and challenges |
title_auth |
Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges |
abstract |
Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. |
abstractGer |
Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. |
abstract_unstemmed |
Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field. |
collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U FID-BIODIV SSG-OLC-PHA GBV_ILN_73 |
title_short |
Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges |
url |
https://doi.org/10.1016/j.gde.2017.01.017 |
remote_bool |
true |
author2 |
Beck, Stephan |
author2Str |
Beck, Stephan |
ppnlink |
ELV022997628 |
mediatype_str_mv |
z |
isOA_txt |
false |
hochschulschrift_bool |
false |
author2_role |
oth |
doi_str |
10.1016/j.gde.2017.01.017 |
up_date |
2024-07-06T17:42:14.894Z |
_version_ |
1803852431906308096 |
fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV040524299</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230625232106.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2017 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.gde.2017.01.017</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2017016000012.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV040524299</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S0959-437X(17)30018-7</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">610</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">660</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">610</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">580</subfield><subfield code="a">540</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">BIODIV</subfield><subfield code="q">DE-30</subfield><subfield code="2">fid</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">42.00</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Tanić, Miljana</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Epigenome-wide association studies for cancer biomarker discovery in circulating cell-free DNA: technical advances and challenges</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2017transfer abstract</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">8</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Since introducing the concept of epigenome-wide association studies (EWAS) in 2011, there has been a vast increase in the number of published EWAS studies in common diseases, including in cancer. These studies have increased our understanding of epigenetic events underlying carcinogenesis and have enabled the discovery of cancer-specific methylation biomarkers. In this mini-review, we have focused on the state of the art in EWAS applied to cell-free circulating DNA for epigenetic biomarker discovery in cancer and discussed associated technical advances and challenges, and our expectations for the future of the field.</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Beck, Stephan</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier</subfield><subfield code="a">George, T. ELSEVIER</subfield><subfield code="t">Hybrid carbon fiber composite lattice truss structures</subfield><subfield code="d">2014transfer abstract</subfield><subfield code="d">reviews of all advances : evaluation of key references : comprehensive listing of papers</subfield><subfield code="g">Amsterdam</subfield><subfield code="w">(DE-627)ELV022997628</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:42</subfield><subfield code="g">year:2017</subfield><subfield code="g">pages:48-55</subfield><subfield code="g">extent:8</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.gde.2017.01.017</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">FID-BIODIV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-PHA</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_73</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">42.00</subfield><subfield code="j">Biologie: Allgemeines</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">42</subfield><subfield code="j">2017</subfield><subfield code="h">48-55</subfield><subfield code="g">8</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">610</subfield></datafield></record></collection>
|
score |
7.3979836 |