271 related articles for article (PubMed ID: 22797899)
21. GenomeChronicler: The Personal Genome Project UK Genomic Report Generator Pipeline.
Guerra-Assunção JA; Conde L; Moghul I; Webster AP; Ecker S; Chervova O; Chatzipantsiou C; Prieto PP; Beck S; Herrero J
Front Genet; 2020; 11():518644. PubMed ID: 33193602
[TBL] [Abstract][Full Text] [Related]
22. Family genome browser: visualizing genomes with pedigree information.
Juan L; Liu Y; Wang Y; Teng M; Zang T; Wang Y
Bioinformatics; 2015 Jul; 31(14):2262-8. PubMed ID: 25788626
[TBL] [Abstract][Full Text] [Related]
23. Gene Variant Databases and Sharing: Creating a Global Genomic Variant Database for Personalized Medicine.
Bean LJ; Hegde MR
Hum Mutat; 2016 Jun; 37(6):559-63. PubMed ID: 26931283
[TBL] [Abstract][Full Text] [Related]
24. The whole genome sequences and experimentally phased haplotypes of over 100 personal genomes.
Mao Q; Ciotlos S; Zhang RY; Ball MP; Chin R; Carnevali P; Barua N; Nguyen S; Agarwal MR; Clegg T; Connelly A; Vandewege W; Zaranek AW; Estep PW; Church GM; Drmanac R; Peters BA
Gigascience; 2016 Oct; 5(1):42. PubMed ID: 27724973
[TBL] [Abstract][Full Text] [Related]
25. Genomic and personalized medicine: foundations and applications.
Ginsburg GS; Willard HF
Transl Res; 2009 Dec; 154(6):277-87. PubMed ID: 19931193
[TBL] [Abstract][Full Text] [Related]
26. Multiple personal genomes await.
Venter JC
Nature; 2010 Apr; 464(7289):676-7. PubMed ID: 20360717
[No Abstract] [Full Text] [Related]
27. Canadian Open Genetics Repository (COGR): a unified clinical genomics database as a community resource for standardising and sharing genetic interpretations.
Lerner-Ellis J; Wang M; White S; Lebo MS;
J Med Genet; 2015 Jul; 52(7):438-45. PubMed ID: 25904639
[TBL] [Abstract][Full Text] [Related]
28. Increasing precision in medicine - tackling the bottleneck of variant interpretation.
Baker M
Drugs Today (Barc); 2016 Jul; 52(7):395-8. PubMed ID: 27540598
[TBL] [Abstract][Full Text] [Related]
29. KNOWLEDGE DRIVEN BINNING AND PHEWAS ANALYSIS IN MARSHFIELD PERSONALIZED MEDICINE RESEARCH PROJECT USING BIOBIN.
Basile AO; Wallace JR; Peissig P; McCarty CA; Brilliant M; Ritchie MD
Pac Symp Biocomput; 2016; 21():249-60. PubMed ID: 26776191
[TBL] [Abstract][Full Text] [Related]
30. A method for scoring the cell type-specific impacts of noncoding variants in personal genomes.
Li W; Duren Z; Jiang R; Wong WH
Proc Natl Acad Sci U S A; 2020 Sep; 117(35):21364-21372. PubMed ID: 32817564
[TBL] [Abstract][Full Text] [Related]
31. ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene-level specification of the ACMG/AMP guidelines for sequence variant interpretation.
Rivera-Muñoz EA; Milko LV; Harrison SM; Azzariti DR; Kurtz CL; Lee K; Mester JL; Weaver MA; Currey E; Craigen W; Eng C; Funke B; Hegde M; Hershberger RE; Mao R; Steiner RD; Vincent LM; Martin CL; Plon SE; Ramos E; Rehm HL; Watson M; Berg JS
Hum Mutat; 2018 Nov; 39(11):1614-1622. PubMed ID: 30311389
[TBL] [Abstract][Full Text] [Related]
32. An integrated framework for reporting clinically relevant biomarkers from paired tumor/normal genomic and transcriptomic sequencing data in support of clinical trials in personalized medicine.
Nasser S; Kurdolgu AA; Izatt T; Aldrich J; Russell ML; Christoforides A; Tembe W; Keifer JA; Corneveaux JJ; Byron SA; Forman KM; Zuccaro C; Keats JJ; Lorusso PM; Carpten JD; Trent JM; Craig DW
Pac Symp Biocomput; 2015; ():56-67. PubMed ID: 25592568
[TBL] [Abstract][Full Text] [Related]
33. The use of PanDrugs to prioritize anticancer drug treatments in a case of T-ALL based on individual genomic data.
Fernández-Navarro P; López-Nieva P; Piñeiro-Yañez E; Carreño-Tarragona G; Martinez-López J; Sánchez Pérez R; Aroca Á; Al-Shahrour F; Cobos-Fernández MÁ; Fernández-Piqueras J
BMC Cancer; 2019 Oct; 19(1):1005. PubMed ID: 31655559
[TBL] [Abstract][Full Text] [Related]
34. The future of Cochrane Neonatal.
Soll RF; Ovelman C; McGuire W
Early Hum Dev; 2020 Nov; 150():105191. PubMed ID: 33036834
[TBL] [Abstract][Full Text] [Related]
35. A variant by any name: quantifying annotation discordance across tools and clinical databases.
Yen JL; Garcia S; Montana A; Harris J; Chervitz S; Morra M; West J; Chen R; Church DM
Genome Med; 2017 Jan; 9(1):7. PubMed ID: 28122645
[TBL] [Abstract][Full Text] [Related]
36. The DNA of a nation.
Marx V
Nature; 2015 Aug; 524(7566):503-5. PubMed ID: 26310768
[No Abstract] [Full Text] [Related]
37. wANNOVAR: annotating genetic variants for personal genomes via the web.
Chang X; Wang K
J Med Genet; 2012 Jul; 49(7):433-6. PubMed ID: 22717648
[TBL] [Abstract][Full Text] [Related]
38. [Detection and interpretation of somatic variants in molecular pathology].
Merkelbach-Bruse S; Rehker J; Siemanowski J; Klauschen F
Pathologe; 2019 May; 40(3):243-249. PubMed ID: 31037375
[TBL] [Abstract][Full Text] [Related]
39. Interpretome: a freely available, modular, and secure personal genome interpretation engine.
Karczewski KJ; Tirrell RP; Cordero P; Tatonetti NP; Dudley JT; Salari K; Snyder M; Altman RB; Kim SK
Pac Symp Biocomput; 2012; ():339-350. PubMed ID: 22174289
[TBL] [Abstract][Full Text] [Related]
40. Precision medicine at the crossroads.
Olson MV
Hum Genomics; 2017 Oct; 11(1):23. PubMed ID: 29020978
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]