70 related articles for article (PubMed ID: 29808933)
1. Clinical-grade validation of whole genome sequencing reveals robust detection of low-frequency variants and copy number alterations in CLL.
Klintman J; Barmpouti K; Knight SJL; Robbe P; Dreau H; Clifford R; Ridout K; Burns A; Timbs A; Bruce D; Antoniou P; Sosinsky A; Becq J; Bentley D; Hillmen P; Taylor JC; Caulfield M; Schuh AH
Br J Haematol; 2018 Aug; 182(3):412-417. PubMed ID: 29808933
[TBL] [Abstract][Full Text] [Related]
2. Analytical and Clinical Validation of a Target-Enhanced Whole Genome Sequencing-Based Comprehensive Genomic Profiling Test.
Ferguson S; Sriram S; Wallace JK; Lee J; Kim JA; Lee Y; Oh BB; Lee WC; Lee S; Connolly-Strong E
Cancer Invest; 2024 May; 42(5):390-399. PubMed ID: 38773925
[TBL] [Abstract][Full Text] [Related]
3. Inferring clonal heterogeneity in cancer using SNP arrays and whole genome sequencing.
Zucker MR; Abruzzo LV; Herling CD; Barron LL; Keating MJ; Abrams ZB; Heerema N; Coombes KR
Bioinformatics; 2019 Sep; 35(17):2924-2931. PubMed ID: 30689715
[TBL] [Abstract][Full Text] [Related]
4. Characterization of Somatically-Acquired Copy Number Alterations in Chronic Lymphocytic Leukaemia Using Shallow Whole Genome Sequencing.
Parker H; Carr L; Syeda S; Bryant D; Strefford JC
Methods Mol Biol; 2019; 1881():327-353. PubMed ID: 30350215
[TBL] [Abstract][Full Text] [Related]
5. Assessing reproducibility of inherited variants detected with short-read whole genome sequencing.
Pan B; Ren L; Onuchic V; Guan M; Kusko R; Bruinsma S; Trigg L; Scherer A; Ning B; Zhang C; Glidewell-Kenney C; Xiao C; Donaldson E; Sedlazeck FJ; Schroth G; Yavas G; Grunenwald H; Chen H; Meinholz H; Meehan J; Wang J; Yang J; Foox J; Shang J; Miclaus K; Dong L; Shi L; Mohiyuddin M; Pirooznia M; Gong P; Golshani R; Wolfinger R; Lababidi S; Sahraeian SME; Sherry S; Han T; Chen T; Shi T; Hou W; Ge W; Zou W; Guo W; Bao W; Xiao W; Fan X; Gondo Y; Yu Y; Zhao Y; Su Z; Liu Z; Tong W; Xiao W; Zook JM; Zheng Y; Hong H
Genome Biol; 2022 Jan; 23(1):2. PubMed ID: 34980216
[TBL] [Abstract][Full Text] [Related]
6. Whole-genome sequencing of chronic lymphocytic leukemia identifies subgroups with distinct biological and clinical features.
Robbe P; Ridout KE; Vavoulis DV; Dréau H; Kinnersley B; Denny N; Chubb D; Appleby N; Cutts A; Cornish AJ; Lopez-Pascua L; Clifford R; Burns A; Stamatopoulos B; Cabes M; Alsolami R; Antoniou P; Oates M; Cavalieri D; ; ; Gibson J; Prabhu AV; Schwessinger R; Jennings D; James T; Maheswari U; Duran-Ferrer M; Carninci P; Knight SJL; Månsson R; Hughes J; Davies J; Ross M; Bentley D; Strefford JC; Devereux S; Pettitt AR; Hillmen P; Caulfield MJ; Houlston RS; Martín-Subero JI; Schuh A
Nat Genet; 2022 Nov; 54(11):1675-1689. PubMed ID: 36333502
[TBL] [Abstract][Full Text] [Related]
7. Comprehensive characterization of human genome variation by high coverage whole-genome sequencing of forty four Caucasians.
Shen H; Li J; Zhang J; Xu C; Jiang Y; Wu Z; Zhao F; Liao L; Chen J; Lin Y; Tian Q; Papasian CJ; Deng HW
PLoS One; 2013; 8(4):e59494. PubMed ID: 23577066
[TBL] [Abstract][Full Text] [Related]
8. ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data.
Minoche AE; Lundie B; Peters GB; Ohnesorg T; Pinese M; Thomas DM; Zankl A; Roscioli T; Schonrock N; Kummerfeld S; Burnett L; Dinger ME; Cowley MJ
Genome Med; 2021 Feb; 13(1):32. PubMed ID: 33632298
[TBL] [Abstract][Full Text] [Related]
9. [Expert consensus on the test development and preliminary implementation of whole genome sequencing for fetal structural abnormalities].
Cyto And Genomics Group Of Medical Genetics Branch Of Chinese Medical Association ; Writing Group For Expert Consensus On Whole-Genome Sequencing In Prenatal Diagnosis ; Wang Y; Zhu X; Sun L; Tang X; Liu N; Kong X
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Jun; 41(6):677-684. PubMed ID: 38818551
[TBL] [Abstract][Full Text] [Related]
10. Recommendations for whole genome sequencing in diagnostics for rare diseases.
Souche E; Beltran S; Brosens E; Belmont JW; Fossum M; Riess O; Gilissen C; Ardeshirdavani A; Houge G; van Gijn M; Clayton-Smith J; Synofzik M; de Leeuw N; Deans ZC; Dincer Y; Eck SH; van der Crabben S; Balasubramanian M; Graessner H; Sturm M; Firth H; Ferlini A; Nabbout R; De Baere E; Liehr T; Macek M; Matthijs G; Scheffer H; Bauer P; Yntema HG; Weiss MM
Eur J Hum Genet; 2022 Sep; 30(9):1017-1021. PubMed ID: 35577938
[TBL] [Abstract][Full Text] [Related]
11. Robust and accurate estimation of paralog-specific copy number for duplicated genes using whole-genome sequencing.
Prodanov T; Bansal V
Nat Commun; 2022 Jun; 13(1):3221. PubMed ID: 35680869
[TBL] [Abstract][Full Text] [Related]
12. Exploring quantitative traits-associated copy number deletions through reanalysis of UK10K consortium whole genome sequencing cohorts.
Lee S; Kim J; Ohn JH
BMC Genomics; 2023 Dec; 24(1):787. PubMed ID: 38110883
[TBL] [Abstract][Full Text] [Related]
13. Integrative NGS testing reveals clonal dynamics of adverse genomic defects contributing to a natural progression in treatment-naïve CLL patients.
Navrkalova V; Plevova K; Radova L; Porc J; Pal K; Malcikova J; Pavlova S; Doubek M; Panovska A; Kotaskova J; Pospisilova S
Br J Haematol; 2024 Jan; 204(1):240-249. PubMed ID: 38062779
[TBL] [Abstract][Full Text] [Related]
14. Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients.
Stranneheim H; Lagerstedt-Robinson K; Magnusson M; Kvarnung M; Nilsson D; Lesko N; Engvall M; Anderlid BM; Arnell H; Johansson CB; Barbaro M; Björck E; Bruhn H; Eisfeldt J; Freyer C; Grigelioniene G; Gustavsson P; Hammarsjö A; Hellström-Pigg M; Iwarsson E; Jemt A; Laaksonen M; Enoksson SL; Malmgren H; Naess K; Nordenskjöld M; Oscarson M; Pettersson M; Rasi C; Rosenbaum A; Sahlin E; Sardh E; Stödberg T; Tesi B; Tham E; Thonberg H; Töhönen V; von Döbeln U; Vassiliou D; Vonlanthen S; Wikström AC; Wincent J; Winqvist O; Wredenberg A; Ygberg S; Zetterström RH; Marits P; Soller MJ; Nordgren A; Wirta V; Lindstrand A; Wedell A
Genome Med; 2021 Mar; 13(1):40. PubMed ID: 33726816
[TBL] [Abstract][Full Text] [Related]
15. Genome sequencing detects a wide range of clinically relevant copy-number variants and other genomic alterations.
James KN; Chowdhury S; Ding Y; Batalov S; Watkins K; Kwon YH; Van Der Kraan L; Ellsworth K; Kingsmore SF; Guidugli L
Genet Med; 2024 Jan; 26(1):101006. PubMed ID: 37869996
[TBL] [Abstract][Full Text] [Related]
16. A novel strategy for clustering major depression individuals using whole-genome sequencing variant data.
Yu C; Baune BT; Licinio J; Wong ML
Sci Rep; 2017 Mar; 7():44389. PubMed ID: 28287625
[TBL] [Abstract][Full Text] [Related]
17. Genome-Wide DNA Alterations in X-Irradiated Human Gingiva Fibroblasts.
Nath N; Hagenau L; Weiss S; Tzvetkova A; Jensen LR; Kaderali L; Port M; Scherthan H; Kuss AW
Int J Mol Sci; 2020 Aug; 21(16):. PubMed ID: 32806598
[TBL] [Abstract][Full Text] [Related]
18. Comprehensive whole-genome sequence analyses provide insights into the genomic architecture of cerebral palsy.
Fehlings DL; Zarrei M; Engchuan W; Sondheimer N; Thiruvahindrapuram B; MacDonald JR; Higginbotham EJ; Thapa R; Behlim T; Aimola S; Switzer L; Ng P; Wei J; Danthi PS; Pellecchia G; Lamoureux S; Ho K; Pereira SL; de Rijke J; Sung WWL; Mowjoodi A; Howe JL; Nalpathamkalam T; Manshaei R; Ghaffari S; Whitney J; Patel RV; Hamdan O; Shaath R; Trost B; Knights S; Samdup D; McCormick A; Hunt C; Kirton A; Kawamura A; Mesterman R; Gorter JW; Dlamini N; Merico D; Hilali M; Hirschfeld K; Grover K; Bautista NX; Han K; Marshall CR; Yuen RKC; Subbarao P; Azad MB; Turvey SE; Mandhane P; Moraes TJ; Simons E; Maxwell G; Shevell M; Costain G; Michaud JL; Hamdan FF; Gauthier J; Uguen K; Stavropoulos DJ; Wintle RF; Oskoui M; Scherer SW
Nat Genet; 2024 Apr; 56(4):585-594. PubMed ID: 38553553
[TBL] [Abstract][Full Text] [Related]
19. A practical guide for mutational signature analysis in hematological malignancies.
Maura F; Degasperi A; Nadeu F; Leongamornlert D; Davies H; Moore L; Royo R; Ziccheddu B; Puente XS; Avet-Loiseau H; Campbell PJ; Nik-Zainal S; Campo E; Munshi N; Bolli N
Nat Commun; 2019 Jul; 10(1):2969. PubMed ID: 31278357
[TBL] [Abstract][Full Text] [Related]
20. Analytical demands to use whole-genome sequencing in precision oncology.
Meggendorfer M; Jobanputra V; Wrzeszczynski KO; Roepman P; de Bruijn E; Cuppen E; Buttner R; Caldas C; Grimmond S; Mullighan CG; Elemento O; Rosenquist R; Schuh A; Haferlach T
Semin Cancer Biol; 2022 Sep; 84():16-22. PubMed ID: 34119643
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
