Genome-Wide Cell-Free DNA Screening: A Focus on Copy-Number Variants EDITORIAL COMMENT

被引：0
|
作者：
Norton, Mary E.
机构：
来源：
OBSTETRICAL & GYNECOLOGICAL SURVEY | 2022年 / 77卷 / 04期
关键词：
D O I：
10.1097/01.ogx.0000827236.19740.69
中图分类号：
R71 [妇产科学];
学科分类号：
100211 ;
摘要：
引用
收藏
页码：196 / 198
页数：3
相关论文
共 50 条
  • [1] Genome-wide cell-free DNA screening: a focus on copy-number variants
    Rafalko, Jill
    Soster, Erica
    Caldwell, Samantha
    Almasri, Eyad
    Westover, Thomas
    Weinblatt, Vivian
    Cacheris, Philip
    GENETICS IN MEDICINE, 2021, 23 (10) : 1847 - 1853
  • [2] Curation and reporting of pathogenic genome-wide copy-number variants in a prenatal cell-free DNA screen
    Cox, Samuel G.
    Acevedo, Ashley
    Ahuja, Anand
    Labreche, Heather G.
    Alfaro, Maria P.
    Pierson, Summer
    Westover, Thomas
    Ratzel, Sarah
    Hancock, Susan
    Moyer, Krista
    Muzzey, Dale
    GENETICS IN MEDICINE, 2025, 27 (01)
  • [3] Genome-wide Sequencing of Cell-free DNA Enables Detection of Copy-number Alterations in Patients with Cancer Where Tissue Biopsy is Not Feasible
    Jensen, Taylor J.
    Goodman, Aaron M.
    Ellison, Christopher K.
    Holden, Kimberly A.
    Kato, Shumei
    Kim, Lisa
    Daniels, Gregory A.
    Fitzgerald, Kerry
    McCarthy, Erin
    Nakashe, Prachi
    Mazloom, Amin R.
    Almasri, Eyad
    McLennan, Graham
    Grosu, Daniel S.
    Eisenberg, Marcia
    Kurzrock, Razelle
    MOLECULAR CANCER THERAPEUTICS, 2021, 20 (11) : 2274 - 2279
  • [4] Genome-Wide Sequencing of Cell-Free DNA Identifies Copy-Number Alterations That Can Be Used for Monitoring Response to Immunotherapy in Cancer Patients
    Jensen, Taylor J.
    Goodman, Aaron M.
    Kato, Shumei
    Ellison, Christopher K.
    Daniels, Gregory A.
    Kim, Lisa
    Nakashe, Prachi
    McCarthy, Erin
    Mazloom, Amin R.
    McLennan, Graham
    Grosu, Daniel S.
    Ehrich, Mathias
    Kurzrock, Razelle
    MOLECULAR CANCER THERAPEUTICS, 2019, 18 (02) : 448 - 458
  • [5] Three years of clinical experience with a genome-wide cfDNA screening test for aneuploidies and copy-number variants
    Soster, Erica
    Boomer, Theresa
    Hicks, Susan
    Caldwell, Samantha
    Dyr, Brittany
    Chibuk, Jason
    Almasri, Eyad
    GENETICS IN MEDICINE, 2021, 23 (07) : 1349 - 1355
  • [6] Genome-wide map of mouse DNA copy number variants
    Eis, Peggy S.
    Graubert, Timothy
    Cahan, Patrick
    Edwin, Deepa
    Selzer, Rebecca
    Richmond, Todd
    Shannon, William
    Li, Xia
    McLeod, Howard
    Cheverud, James
    Ley, Timothy
    CELLULAR ONCOLOGY, 2007, 29 (02) : 124 - 124
  • [7] Genome-wide analysis of DNA copy-number changes using cDNA microarrays
    Pollack, JR
    Perou, CM
    Alizadeh, AA
    Eisen, MB
    Pergamenschikov, A
    Williams, CF
    Jeffrey, SS
    Botstein, D
    Brown, PO
    NATURE GENETICS, 1999, 23 (01) : 41 - 46
  • [8] Genome-wide analysis of DNA copy-number changes using cDNA microarrays
    Jonathan R. Pollack
    Charles M. Perou
    Ash A. Alizadeh
    Michael B. Eisen
    Alexander Pergamenschikov
    Cheryl F. Williams
    Stefanie S. Jeffrey
    David Botstein
    Patrick O. Brown
    Nature Genetics, 1999, 23 : 41 - 46
  • [9] Genome-Wide Analysis of Circulating Cell-Free DNA Copy Number Detects Active Melanoma and Predicts Survival
    Silva, Shobha
    Danson, Sarah
    Teare, Dawn
    Taylor, Fiona
    Bradford, James
    McDonagh, Andrew J. G.
    Salawu, Abdulazeez
    Wells, Greg
    Burghel, George J.
    Brock, Ian
    Connley, Daniel
    Cramp, Helen
    Hughes, David
    Tiffin, Nick
    Cox, Angela
    CLINICAL CHEMISTRY, 2018, 64 (09) : 1338 - 1346
  • [10] Detection of genome-wide copy number alterations in tumor tissue and cell-free DNA of pancreatic cancer patients
    Wieme, G.
    Berrevoet, F.
    Vanlander, A.
    Van Dorpe, J.
    Hoorens, A.
    Van der Linden, M.
    Parton, B.
    Van Limmen, J.
    De Bruyne, A.
    De Man, M.
    Geboes, K.
    Claes, K. B. M.
    EUROPEAN JOURNAL OF HUMAN GENETICS, 2019, 27 : 1593 - 1594
12345