Plasma DNA End-Motif Profiling as a Fragmentomic Marker in Cancer, Pregnancy, and Transplantation

Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without H...

Full description

Saved in:
Bibliographic Details
Published inCancer discovery Vol. 10; no. 5; pp. 664 - 673
Main Authors Jiang, Peiyong, Sun, Kun, Peng, Wenlei, Cheng, Suk Hang, Ni, Meng, Yeung, Philip C., Heung, Macy M.S., Xie, Tingting, Shang, Huimin, Zhou, Ze, Chan, Rebecca W.Y., Wong, John, Wong, Vincent W.S., Poon, Liona C., Leung, Tak Yeung, Lam, W.K. Jacky, Chan, Jason Y.K., Chan, Henry L.Y., Chan, K.C. Allen, Chiu, Rossa W.K., Lo, Y.M. Dennis
Format Journal Article
LanguageEnglish
Published United States 01.05.2020
Online AccessGet full text

Cover

Loading…
Abstract Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without HCC, patients with HCC showed a preferential pattern of 4-mer end motifs. In particular, the abundance of plasma DNA motif CCCA was much lower in patients with HCC than in subjects without HCC. The aberrant end motifs were also observed in patients with other cancer types, including colorectal cancer, lung cancer, nasopharyngeal carcinoma, and head and neck squamous cell carcinoma. We further observed that the profile of plasma DNA end motifs originating from the same organ, such as the liver, placenta, and hematopoietic cells, generally clustered together. The profile of end motifs may therefore serve as a class of biomarkers for liquid biopsy in oncology, noninvasive prenatal testing, and transplantation monitoring. SIGNIFICANCE: Plasma DNA molecules originating from the liver, HCC and other cancers, placenta, and hematopoietic cells each harbor a set of characteristic plasma DNA end motifs. Such markers carry tissue-of-origin information and represent a new class of biomarkers in the nascent field of fragmentomics. .
AbstractList Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without HCC, patients with HCC showed a preferential pattern of 4-mer end motifs. In particular, the abundance of plasma DNA motif CCCA was much lower in patients with HCC than in subjects without HCC. The aberrant end motifs were also observed in patients with other cancer types, including colorectal cancer, lung cancer, nasopharyngeal carcinoma, and head and neck squamous cell carcinoma. We further observed that the profile of plasma DNA end motifs originating from the same organ, such as the liver, placenta, and hematopoietic cells, generally clustered together. The profile of end motifs may therefore serve as a class of biomarkers for liquid biopsy in oncology, noninvasive prenatal testing, and transplantation monitoring. SIGNIFICANCE: Plasma DNA molecules originating from the liver, HCC and other cancers, placenta, and hematopoietic cells each harbor a set of characteristic plasma DNA end motifs. Such markers carry tissue-of-origin information and represent a new class of biomarkers in the nascent field of fragmentomics. .
Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without HCC, patients with HCC showed a preferential pattern of 4-mer end motifs. In particular, the abundance of plasma DNA motif CCCA was much lower in patients with HCC than in subjects without HCC. The aberrant end motifs were also observed in patients with other cancer types, including colorectal cancer, lung cancer, nasopharyngeal carcinoma, and head and neck squamous cell carcinoma. We further observed that the profile of plasma DNA end motifs originating from the same organ, such as the liver, placenta, and hematopoietic cells, generally clustered together. The profile of end motifs may therefore serve as a class of biomarkers for liquid biopsy in oncology, noninvasive prenatal testing, and transplantation monitoring. SIGNIFICANCE: Plasma DNA molecules originating from the liver, HCC and other cancers, placenta, and hematopoietic cells each harbor a set of characteristic plasma DNA end motifs. Such markers carry tissue-of-origin information and represent a new class of biomarkers in the nascent field of fragmentomics.This article is highlighted in the In This Issue feature, p. 627.Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a significant increase in the diversity of plasma DNA end motifs in patients with hepatocellular carcinoma (HCC). Compared with patients without HCC, patients with HCC showed a preferential pattern of 4-mer end motifs. In particular, the abundance of plasma DNA motif CCCA was much lower in patients with HCC than in subjects without HCC. The aberrant end motifs were also observed in patients with other cancer types, including colorectal cancer, lung cancer, nasopharyngeal carcinoma, and head and neck squamous cell carcinoma. We further observed that the profile of plasma DNA end motifs originating from the same organ, such as the liver, placenta, and hematopoietic cells, generally clustered together. The profile of end motifs may therefore serve as a class of biomarkers for liquid biopsy in oncology, noninvasive prenatal testing, and transplantation monitoring. SIGNIFICANCE: Plasma DNA molecules originating from the liver, HCC and other cancers, placenta, and hematopoietic cells each harbor a set of characteristic plasma DNA end motifs. Such markers carry tissue-of-origin information and represent a new class of biomarkers in the nascent field of fragmentomics.This article is highlighted in the In This Issue feature, p. 627.
Author Cheng, Suk Hang
Heung, Macy M.S.
Wong, Vincent W.S.
Lo, Y.M. Dennis
Ni, Meng
Leung, Tak Yeung
Lam, W.K. Jacky
Yeung, Philip C.
Chan, Jason Y.K.
Chan, Rebecca W.Y.
Sun, Kun
Shang, Huimin
Wong, John
Chan, Henry L.Y.
Xie, Tingting
Zhou, Ze
Chan, K.C. Allen
Jiang, Peiyong
Peng, Wenlei
Poon, Liona C.
Chiu, Rossa W.K.
Author_xml – sequence: 1
  givenname: Peiyong
  surname: Jiang
  fullname: Jiang, Peiyong
– sequence: 2
  givenname: Kun
  surname: Sun
  fullname: Sun, Kun
– sequence: 3
  givenname: Wenlei
  surname: Peng
  fullname: Peng, Wenlei
– sequence: 4
  givenname: Suk Hang
  surname: Cheng
  fullname: Cheng, Suk Hang
– sequence: 5
  givenname: Meng
  orcidid: 0000-0002-5565-0639
  surname: Ni
  fullname: Ni, Meng
– sequence: 6
  givenname: Philip C.
  orcidid: 0000-0003-4960-1491
  surname: Yeung
  fullname: Yeung, Philip C.
– sequence: 7
  givenname: Macy M.S.
  surname: Heung
  fullname: Heung, Macy M.S.
– sequence: 8
  givenname: Tingting
  surname: Xie
  fullname: Xie, Tingting
– sequence: 9
  givenname: Huimin
  surname: Shang
  fullname: Shang, Huimin
– sequence: 10
  givenname: Ze
  surname: Zhou
  fullname: Zhou, Ze
– sequence: 11
  givenname: Rebecca W.Y.
  orcidid: 0000-0002-9480-4637
  surname: Chan
  fullname: Chan, Rebecca W.Y.
– sequence: 12
  givenname: John
  surname: Wong
  fullname: Wong, John
– sequence: 13
  givenname: Vincent W.S.
  surname: Wong
  fullname: Wong, Vincent W.S.
– sequence: 14
  givenname: Liona C.
  surname: Poon
  fullname: Poon, Liona C.
– sequence: 15
  givenname: Tak Yeung
  surname: Leung
  fullname: Leung, Tak Yeung
– sequence: 16
  givenname: W.K. Jacky
  surname: Lam
  fullname: Lam, W.K. Jacky
– sequence: 17
  givenname: Jason Y.K.
  orcidid: 0000-0002-9480-4637
  surname: Chan
  fullname: Chan, Jason Y.K.
– sequence: 18
  givenname: Henry L.Y.
  orcidid: 0000-0002-9480-4637
  surname: Chan
  fullname: Chan, Henry L.Y.
– sequence: 19
  givenname: K.C. Allen
  orcidid: 0000-0003-1780-1691
  surname: Chan
  fullname: Chan, K.C. Allen
– sequence: 20
  givenname: Rossa W.K.
  orcidid: 0000-0001-8207-9207
  surname: Chiu
  fullname: Chiu, Rossa W.K.
– sequence: 21
  givenname: Y.M. Dennis
  orcidid: 0000-0001-8746-0293
  surname: Lo
  fullname: Lo, Y.M. Dennis
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32111602$$D View this record in MEDLINE/PubMed
BookMark eNp9kUlPwzAQhS0Eoiz9Bwj5yIGAlyw1N5SySWyHcrYmzrgyJE6x00P_PalaeuDAXGY0-t5o9N4x2fedR0LOOLviPJtcC56pZCIUuyqnCVcJy4XYI0e79f5uLtIRGcf4yYZKVZqx4pCMpOCc50wcEXhvILZAp6-39M7XyUvXO0vfQ2dd4_ycQqRA7wPMW_R91zpDXyB8YaDO0xK8wXA50Dj3w7y6pOBrOgvg46IB30PvOn9KDiw0EcfbfkI-7u9m5WPy_PbwVN4-J0YWsk8sYp5ZZVIQrFKqLpiRDGRuucU0kwC8lpU1iExUuUQBTMpMqqrASSWFyOQJudjcXYTue4mx162LBpvhEeyWUQuZqzTN8wkb0PMtuqxarPUiuBbCSv_aMgDpBjChizGg3SGc6XUAeu2uXjuty6nmSq8DGGQ3f2TGbUzoA7jmf_EPRm2Jag
CitedBy_id crossref_primary_10_1007_s00432_023_05521_4
crossref_primary_10_1016_j_tranon_2023_101694
crossref_primary_10_1038_s41467_024_50850_8
crossref_primary_10_1038_s41586_023_06903_x
crossref_primary_10_1101_gr_279667_124
crossref_primary_10_1186_s13059_022_02710_1
crossref_primary_10_1093_clinchem_hvae118
crossref_primary_10_3390_diagnostics12040870
crossref_primary_10_7717_peerj_14303
crossref_primary_10_1016_j_ccell_2025_02_002
crossref_primary_10_1016_j_xpro_2024_103357
crossref_primary_10_1038_s41598_022_05606_z
crossref_primary_10_1038_s41467_024_55594_z
crossref_primary_10_1073_pnas_2114937118
crossref_primary_10_1016_j_jhep_2023_11_030
crossref_primary_10_3390_cancers15010096
crossref_primary_10_3389_fonc_2024_1332004
crossref_primary_10_1186_s12943_022_01551_7
crossref_primary_10_3389_fimmu_2022_1001690
crossref_primary_10_1016_j_canlet_2024_217216
crossref_primary_10_1101_gr_278413_123
crossref_primary_10_1186_s13046_024_03067_y
crossref_primary_10_3390_cancers13225615
crossref_primary_10_1016_j_humpath_2024_105679
crossref_primary_10_1093_noajnl_vdac066
crossref_primary_10_1038_s41551_025_01370_3
crossref_primary_10_1101_gr_275691_121
crossref_primary_10_1016_j_cca_2024_120033
crossref_primary_10_1093_clinchem_hvac050
crossref_primary_10_3389_fendo_2023_1164822
crossref_primary_10_1016_j_cca_2024_119729
crossref_primary_10_1093_clinchem_hvac173
crossref_primary_10_1080_14737159_2022_2094706
crossref_primary_10_7554_eLife_89083
crossref_primary_10_7554_eLife_89083_3
crossref_primary_10_1016_j_ebiom_2023_104962
crossref_primary_10_1016_j_jtho_2022_09_109
crossref_primary_10_1016_j_critrevonc_2024_104608
crossref_primary_10_1016_j_crmeth_2024_100793
crossref_primary_10_1038_s41416_022_02048_2
crossref_primary_10_1016_j_trecan_2020_11_001
crossref_primary_10_2217_fon_2022_1218
crossref_primary_10_3389_fonc_2021_662094
crossref_primary_10_1002_pd_5952
crossref_primary_10_1016_j_annonc_2023_06_001
crossref_primary_10_1158_1078_0432_CCR_24_0797
crossref_primary_10_1016_j_coviro_2023_101331
crossref_primary_10_1152_ajplung_00364_2020
crossref_primary_10_3390_jmp4030013
crossref_primary_10_1016_j_tig_2021_04_005
crossref_primary_10_1016_j_xcrm_2023_101349
crossref_primary_10_1038_s41422_020_00457_7
crossref_primary_10_1038_s41467_022_32598_1
crossref_primary_10_1016_j_mcp_2022_101873
crossref_primary_10_1371_journal_pgen_1011484
crossref_primary_10_1016_j_csbj_2024_08_007
crossref_primary_10_1093_clinchem_hvad131
crossref_primary_10_1016_j_esmoop_2024_103595
crossref_primary_10_1164_rccm_202109_2019OC
crossref_primary_10_21926_obm_transplant_2302190
crossref_primary_10_1038_s41598_021_88866_5
crossref_primary_10_1101_gr_275426_121
crossref_primary_10_1002_mco2_329
crossref_primary_10_1073_pnas_2220982120
crossref_primary_10_1186_s12916_024_03531_8
crossref_primary_10_3390_diagnostics12081834
crossref_primary_10_1186_s13073_022_01141_8
crossref_primary_10_1007_s00439_020_02227_2
crossref_primary_10_1016_j_ebiom_2024_105321
crossref_primary_10_3390_ijms24021503
crossref_primary_10_1038_s41467_023_41820_7
crossref_primary_10_1126_scitranslmed_abm6863
crossref_primary_10_1136_gutjnl_2021_325036
crossref_primary_10_1002_1878_0261_13745
crossref_primary_10_1016_j_tig_2024_10_007
crossref_primary_10_1371_journal_pgen_1010262
crossref_primary_10_3390_cancers15072051
crossref_primary_10_1093_clinchem_hvac029
crossref_primary_10_1136_gutjnl_2024_333533
crossref_primary_10_1016_j_ajhg_2023_08_014
crossref_primary_10_1016_j_jhep_2023_05_039
crossref_primary_10_1038_s42003_024_06769_3
crossref_primary_10_1002_1878_0261_12794
crossref_primary_10_1007_s00438_023_02014_4
crossref_primary_10_1007_s12029_022_00906_z
crossref_primary_10_3389_fonc_2023_1127086
crossref_primary_10_1038_s41698_024_00635_5
crossref_primary_10_1073_pnas_2209852119
crossref_primary_10_1038_s41467_022_35076_w
crossref_primary_10_1139_bcb_2024_0004
crossref_primary_10_1002_hep_32308
crossref_primary_10_1016_j_cca_2023_117751
crossref_primary_10_1016_j_xgen_2022_100242
crossref_primary_10_1056_EVIDoa2200309
crossref_primary_10_1186_s13148_022_01420_6
crossref_primary_10_1016_j_ctrv_2024_102774
crossref_primary_10_1038_s41587_021_01207_9
crossref_primary_10_1016_j_celrep_2024_114799
crossref_primary_10_1016_j_xcrm_2024_101664
crossref_primary_10_1186_s40364_023_00524_2
crossref_primary_10_1016_j_xcrm_2024_101660
crossref_primary_10_3390_ijms232214197
crossref_primary_10_1016_j_xcrm_2023_101384
crossref_primary_10_1038_s41698_025_00876_y
crossref_primary_10_1016_j_jlb_2024_100141
crossref_primary_10_1093_clinchem_hvae156
crossref_primary_10_1002_advs_202308243
crossref_primary_10_1089_bio_2022_0004
crossref_primary_10_1016_j_ebiom_2022_104131
crossref_primary_10_1002_ctm2_70225
crossref_primary_10_1093_bib_bbae430
crossref_primary_10_1038_s41571_020_0404_0
crossref_primary_10_1158_2159_8290_CD_22_0692
crossref_primary_10_1016_j_crad_2021_07_005
crossref_primary_10_1158_0008_5472_CAN_23_3486
crossref_primary_10_1136_jitc_2022_006013
crossref_primary_10_1158_2159_8290_CD_21_1252
crossref_primary_10_3748_wjg_v27_i34_5666
crossref_primary_10_1016_j_it_2023_03_005
crossref_primary_10_1016_j_jtcvs_2024_04_026
crossref_primary_10_1038_s41568_025_00795_x
crossref_primary_10_1146_annurev_bioeng_110222_111259
crossref_primary_10_1126_science_abb9601
crossref_primary_10_1186_s12967_024_05326_0
crossref_primary_10_1016_j_crmeth_2024_100877
crossref_primary_10_1186_s13045_021_01189_w
crossref_primary_10_3390_diagnostics12092147
crossref_primary_10_1080_14796694_2024_2413266
crossref_primary_10_1002_ijc_34981
crossref_primary_10_1101_gr_261396_120
crossref_primary_10_1016_j_trecan_2023_08_010
crossref_primary_10_1007_s10637_023_01363_6
crossref_primary_10_1016_j_tranon_2024_102085
crossref_primary_10_1093_clinchem_hvac086
crossref_primary_10_1016_j_ygeno_2023_110662
crossref_primary_10_3390_ijms25063502
crossref_primary_10_1038_s41587_022_01222_4
crossref_primary_10_1186_s12916_023_02954_z
crossref_primary_10_1186_s40001_025_02313_z
crossref_primary_10_1093_clinchem_hvab268
crossref_primary_10_1016_j_ebiom_2023_104553
crossref_primary_10_1186_s13046_025_03348_0
crossref_primary_10_1200_CCI_24_00224
crossref_primary_10_3390_cancers15184556
crossref_primary_10_1016_j_ajhg_2020_09_006
crossref_primary_10_1016_j_xcrm_2023_101281
crossref_primary_10_1093_nar_gkad777
crossref_primary_10_1016_j_tcb_2024_11_007
crossref_primary_10_3390_diagnostics12040978
crossref_primary_10_1186_s12967_024_05416_z
crossref_primary_10_1186_s12859_023_05478_8
crossref_primary_10_3389_fonc_2022_943253
crossref_primary_10_2196_48247
crossref_primary_10_1016_j_eng_2021_02_020
crossref_primary_10_1038_s41598_023_40611_w
crossref_primary_10_1186_s12943_024_01959_3
crossref_primary_10_1002_ctd2_280
crossref_primary_10_1016_j_tig_2023_01_004
crossref_primary_10_1093_clinchem_hvac197
crossref_primary_10_1136_jitc_2022_006284
crossref_primary_10_1016_j_ajg_2024_08_003
crossref_primary_10_1016_j_ygeno_2024_110876
crossref_primary_10_1002_1878_0261_13041
crossref_primary_10_1016_j_gene_2024_148667
crossref_primary_10_1073_pnas_2404058121
crossref_primary_10_1093_clinchem_hvaa325
crossref_primary_10_1186_s12915_023_01752_6
crossref_primary_10_1016_j_jcmgh_2022_02_008
crossref_primary_10_1038_s41467_023_41774_w
crossref_primary_10_1186_s13048_022_01068_z
crossref_primary_10_1093_bib_bbae053
crossref_primary_10_1186_s12920_024_02022_2
crossref_primary_10_1053_j_seminhematol_2023_06_006
crossref_primary_10_1186_s12943_021_01491_8
crossref_primary_10_7554_eLife_64356
crossref_primary_10_1038_s41467_023_35959_6
crossref_primary_10_1002_pd_5978
crossref_primary_10_1126_science_aaw3616
crossref_primary_10_3390_ijms25021243
crossref_primary_10_1002_advs_202309422
Cites_doi 10.1101/gr.242719.118
10.1126/scitranslmed.3007094
10.1016/j.cell.2015.11.050
10.1093/clinchem/48.3.421
10.1073/pnas.1814616115
10.1126/scitranslmed.3001720
10.1186/1471-2164-16-S13-S1
10.1073/pnas.1517494112
10.1126/scitranslmed.aat4921
10.1073/pnas.1815031116
10.1073/pnas.1615800113
10.1073/pnas.1313995110
10.1016/S0140-6736(97)02174-0
10.1373/clinchem.2011.169318
10.1373/clinchem.2016.254813
10.1373/clinchem.2003.024893
10.1073/pnas.1500076112
10.1186/gb-2010-11-10-r106
10.1016/j.ajhg.2020.01.008
10.1038/cr.2017.106
10.1016/S0140-6736(05)79055-3
10.1073/pnas.1508736112
10.1373/clinchem.2016.265702
10.1373/clinchem.2018.290304
ContentType Journal Article
Copyright 2020 American Association for Cancer Research.
Copyright_xml – notice: 2020 American Association for Cancer Research.
DBID AAYXX
CITATION
NPM
7X8
DOI 10.1158/2159-8290.CD-19-0622
DatabaseName CrossRef
PubMed
MEDLINE - Academic
DatabaseTitle CrossRef
PubMed
MEDLINE - Academic
DatabaseTitleList PubMed
MEDLINE - Academic
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 2159-8290
EndPage 673
ExternalDocumentID 32111602
10_1158_2159_8290_CD_19_0622
Genre Research Support, Non-U.S. Gov't
Journal Article
GroupedDBID ---
53G
5VS
AAYXX
ADBBV
ADCOW
AENEX
AFHIN
AFUMD
ALMA_UNASSIGNED_HOLDINGS
BR6
BTFSW
CITATION
EBS
EJD
H13
KQ8
OK1
RCR
RHI
NPM
7X8
ID FETCH-LOGICAL-c373t-fee65f9c4a20b99d70c30a36f1fe453aa1d3bfcee02b63e2a033539b7e8b32253
ISSN 2159-8274
2159-8290
IngestDate Fri Jul 11 06:56:05 EDT 2025
Thu Apr 03 07:00:46 EDT 2025
Tue Jul 01 00:56:27 EDT 2025
Thu Apr 24 23:10:39 EDT 2025
IsPeerReviewed false
IsScholarly true
Issue 5
Language English
License 2020 American Association for Cancer Research.
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c373t-fee65f9c4a20b99d70c30a36f1fe453aa1d3bfcee02b63e2a033539b7e8b32253
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ORCID 0000-0003-1780-1691
0000-0001-8207-9207
0000-0002-9480-4637
0000-0003-4960-1491
0000-0001-8746-0293
0000-0002-5565-0639
PMID 32111602
PQID 2369446680
PQPubID 23479
PageCount 10
ParticipantIDs proquest_miscellaneous_2369446680
pubmed_primary_32111602
crossref_primary_10_1158_2159_8290_CD_19_0622
crossref_citationtrail_10_1158_2159_8290_CD_19_0622
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2020-05-01
2020-05-00
20200501
PublicationDateYYYYMMDD 2020-05-01
PublicationDate_xml – month: 05
  year: 2020
  text: 2020-05-01
  day: 01
PublicationDecade 2020
PublicationPlace United States
PublicationPlace_xml – name: United States
PublicationTitle Cancer discovery
PublicationTitleAlternate Cancer Discov
PublicationYear 2020
References Song (2022060622181420700_bib18) 2017; 27
Sun (2022060622181420700_bib20) 2019; 29
Chan (2022060622181420700_bib7) 2003; 63
De Vlaminck (2022060622181420700_bib11) 2015; 112
Anders (2022060622181420700_bib17) 2010; 11
Jiang (2022060622181420700_bib5) 2018; 115
Zheng (2022060622181420700_bib10) 2012; 58
Yu (2022060622181420700_bib14) 2017; 63
Chan (2022060622181420700_bib1) 2004; 50
Gai (2022060622181420700_bib22) 2018; 64
Sun (2022060622181420700_bib12) 2015; 112
Han (2022060622181420700_bib25) 2020; 106
Chan (2022060622181420700_bib21) 2013; 110
Lo (2022060622181420700_bib8) 1998; 351
Serpas (2022060622181420700_bib16) 2019; 116
Jiang (2022060622181420700_bib24) 2017; 63
Bettegowda (2022060622181420700_bib19) 2014; 6
Ivanov (2022060622181420700_bib6) 2015; 16
Lo (2022060622181420700_bib23) 1997; 350
Jiang (2022060622181420700_bib13) 2015; 112
Mouliere (2022060622181420700_bib15) 2018; 10
Lo (2022060622181420700_bib2) 2010; 2
Snyder (2022060622181420700_bib3) 2016; 164
Lui (2022060622181420700_bib9) 2002; 48
Chan (2022060622181420700_bib4) 2016; 113
References_xml – volume: 29
  start-page: 418
  year: 2019
  ident: 2022060622181420700_bib20
  article-title: Orientation-aware plasma cell-free DNA fragmentation analysis in open chromatin regions informs tissue of origin
  publication-title: Genome Res
  doi: 10.1101/gr.242719.118
– volume: 6
  start-page: iii7
  year: 2014
  ident: 2022060622181420700_bib19
  article-title: Detection of circulating tumor DNA in early- and late-stage human malignancies
  publication-title: Sci Transl Med
  doi: 10.1126/scitranslmed.3007094
– volume: 164
  start-page: 57
  year: 2016
  ident: 2022060622181420700_bib3
  article-title: Cell-free DNA comprises an in vivo nucleosome footprint that informs its tissues-of-origin
  publication-title: Cell
  doi: 10.1016/j.cell.2015.11.050
– volume: 48
  start-page: 421
  year: 2002
  ident: 2022060622181420700_bib9
  article-title: Predominant hematopoietic origin of cell-free dna in plasma and serum after sex-mismatched bone marrow transplantation
  publication-title: Clin Chem
  doi: 10.1093/clinchem/48.3.421
– volume: 115
  start-page: E10925
  year: 2018
  ident: 2022060622181420700_bib5
  article-title: Preferred end coordinates and somatic variants as signatures of circulating tumor DNA associated with hepatocellular carcinoma
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1814616115
– volume: 63
  start-page: 2028
  year: 2003
  ident: 2022060622181420700_bib7
  article-title: Molecular characterization of circulating EBV DNA in the plasma of nasopharyngeal carcinoma and lymphoma patients
  publication-title: Cancer Res
– volume: 2
  start-page: 61ra91
  year: 2010
  ident: 2022060622181420700_bib2
  article-title: Maternal plasma DNA sequencing reveals the genome-wide genetic and mutational profile of the fetus
  publication-title: Sci Transl Med
  doi: 10.1126/scitranslmed.3001720
– volume: 16
  start-page: S1
  year: 2015
  ident: 2022060622181420700_bib6
  article-title: Non-random fragmentation patterns in circulating cell-free DNA reflect epigenetic regulation
  publication-title: BMC Genomics
  doi: 10.1186/1471-2164-16-S13-S1
– volume: 112
  start-page: 13336
  year: 2015
  ident: 2022060622181420700_bib11
  article-title: Noninvasive monitoring of infection and rejection after lung transplantation
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1517494112
– volume: 10
  start-page: eaat4921
  year: 2018
  ident: 2022060622181420700_bib15
  article-title: Enhanced detection of circulating tumor DNA by fragment size analysis
  publication-title: Sci Transl Med
  doi: 10.1126/scitranslmed.aat4921
– volume: 116
  start-page: 641
  year: 2019
  ident: 2022060622181420700_bib16
  article-title: Dnase1l3 deletion causes aberrations in length and end-motif frequencies in plasma DNA
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1815031116
– volume: 113
  start-page: E8159
  year: 2016
  ident: 2022060622181420700_bib4
  article-title: Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1615800113
– volume: 110
  start-page: 18761
  year: 2013
  ident: 2022060622181420700_bib21
  article-title: Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencing
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1313995110
– volume: 350
  start-page: 485
  year: 1997
  ident: 2022060622181420700_bib23
  article-title: Presence of fetal DNA in maternal plasma and serum
  publication-title: Lancet
  doi: 10.1016/S0140-6736(97)02174-0
– volume: 58
  start-page: 549
  year: 2012
  ident: 2022060622181420700_bib10
  article-title: Nonhematopoietically derived DNA is shorter than hematopoietically derived DNA in plasma: a transplantation model
  publication-title: Clin Chem
  doi: 10.1373/clinchem.2011.169318
– volume: 63
  start-page: 495
  year: 2017
  ident: 2022060622181420700_bib14
  article-title: Combined count- and size-based analysis of maternal plasma DNA for noninvasive prenatal detection of fetal subchromosomal aberrations facilitates elucidation of the fetal and/or maternal origin of the aberrations
  publication-title: Clin Chem
  doi: 10.1373/clinchem.2016.254813
– volume: 50
  start-page: 88
  year: 2004
  ident: 2022060622181420700_bib1
  article-title: Size distributions of maternal and fetal DNA in maternal plasma
  publication-title: Clin Chem
  doi: 10.1373/clinchem.2003.024893
– volume: 112
  start-page: E1317
  year: 2015
  ident: 2022060622181420700_bib13
  article-title: Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1500076112
– volume: 11
  start-page: R106
  year: 2010
  ident: 2022060622181420700_bib17
  article-title: Differential expression analysis for sequence count data
  publication-title: Genome Biol
  doi: 10.1186/gb-2010-11-10-r106
– volume: 106
  start-page: 202
  year: 2020
  ident: 2022060622181420700_bib25
  article-title: The biology of cell-free DNA fragmentation and the roles of DNASE1, DNASE1L3, and DFFB
  publication-title: Am J Hum Genet
  doi: 10.1016/j.ajhg.2020.01.008
– volume: 27
  start-page: 1231
  year: 2017
  ident: 2022060622181420700_bib18
  article-title: 5-Hydroxymethylcytosine signatures in cell-free DNA provide information about tumor types and stages
  publication-title: Cell Res
  doi: 10.1038/cr.2017.106
– volume: 351
  start-page: 1329
  year: 1998
  ident: 2022060622181420700_bib8
  article-title: Presence of donor-specific DNA in plasma of kidney and liver-transplant recipients
  publication-title: Lancet
  doi: 10.1016/S0140-6736(05)79055-3
– volume: 112
  start-page: E5503
  year: 2015
  ident: 2022060622181420700_bib12
  article-title: Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments
  publication-title: Proc Natl Acad Sci U S A
  doi: 10.1073/pnas.1508736112
– volume: 63
  start-page: 606
  year: 2017
  ident: 2022060622181420700_bib24
  article-title: Gestational age assessment by methylation and size profiling of maternal plasma DNA: a feasibility study
  publication-title: Clin Chem
  doi: 10.1373/clinchem.2016.265702
– volume: 64
  start-page: 1239
  year: 2018
  ident: 2022060622181420700_bib22
  article-title: Liver- and colon-specific DNA methylation markers in plasma for investigation of colorectal cancers with or without liver metastases
  publication-title: Clin Chem
  doi: 10.1373/clinchem.2018.290304
SSID ssj0000494507
Score 2.6328273
Snippet Plasma DNA fragmentomics is an emerging area of research covering plasma DNA sizes, end points, and nucleosome footprints. In the present study, we found a...
SourceID proquest
pubmed
crossref
SourceType Aggregation Database
Index Database
Enrichment Source
StartPage 664
Title Plasma DNA End-Motif Profiling as a Fragmentomic Marker in Cancer, Pregnancy, and Transplantation
URI https://www.ncbi.nlm.nih.gov/pubmed/32111602
https://www.proquest.com/docview/2369446680
Volume 10
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1bb9MwFLbKkBAviDvlJiPx1rk4duwkj1M7VDF1KmITe4vsxJkiSora5mH8Cf4yPnHqZGNcxktUWelp2vP1-LN9vnMQelvoLEoE5UQYLkmYs5jEhc4J14qZII6KXMNCcX4sZ6fhhzNxNhj86GUt1Vs9zr5fqyv5H6_aMetXUMnewLPeqB2wr61_7dV62F7_yccLS32_qtH0-GB0WOVkvtqWUIEIunA32sPNSAEzPYcdQFAfN8ocs26UfuDtxluLtTmHqhsXu0ROV-98qareKX1XyyCDluLlJoPUzy7_pmy3nRemvFi1k2Fz1NQEtaO66kKwu_GzqZam7JIL2uFP9ZfRTLUG2s0IRrvUPxezLIFISMxc452x6Y-5rqA-6NIeuEQvgkoZ9iZj6fqc_BrnBWgXvOXxZEpAjCWdxvlyWe0r051PQmyWPyJOwUoKVtLJNA2SFKzcQreZXXdA4Dz6GPtNOyimIxoJvv-irRzTGnp33eNcpju_WcM0XObkPrrXLkLwgUPUAzQw1UN0Z96mWTxCygELW2BhDyzsgYXVBivcBxZ2wMJlhR1E9rGH1T62oMJXQPUYnb4_PJnMSNuLg2Q84ltSGCNFkWShYlQnSR7RjFPFZREUJhRcqSDnurCMizItuWGKci54oiMTa5gz-BO0V60q8wzhMIghbhiqizw0loNqLfJCWi5rdGTp7RDx3U-WZm2heuiXskz_5LEhIv5d31yhlr_c_2bnjdRGVDgmU5VZ1ZuUcZlAlkNMh-ipc5O3yJnlBpKy5zf8tBfobvd3eYn2tuvavLJsdqtfNwj7CZr-lgw
linkProvider Colorado Alliance of Research Libraries
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Plasma+DNA+End-Motif+Profiling+as+a+Fragmentomic+Marker+in+Cancer%2C+Pregnancy%2C+and+Transplantation&rft.jtitle=Cancer+discovery&rft.au=Jiang%2C+Peiyong&rft.au=Sun%2C+Kun&rft.au=Peng%2C+Wenlei&rft.au=Cheng%2C+Suk+Hang&rft.date=2020-05-01&rft.issn=2159-8274&rft.eissn=2159-8290&rft.volume=10&rft.issue=5&rft.spage=664&rft.epage=673&rft_id=info:doi/10.1158%2F2159-8290.CD-19-0622&rft.externalDBID=n%2Fa&rft.externalDocID=10_1158_2159_8290_CD_19_0622
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2159-8274&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2159-8274&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2159-8274&client=summon