Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
about
A quantitative comparison of single-cell whole genome amplification methods.Preferential Allele Expression Analysis Identifies Shared Germline and Somatic Driver Genes in Advanced Ovarian Cancer.Measurements of Intrahost Viral Diversity Are Extremely Sensitive to Systematic Errors in Variant Calling.The Impact of Environmental and Endogenous Damage on Somatic Mutation Load in Human Skin FibroblastsA New Chicken Genome Assembly Provides Insight into Avian Genome Structure.A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscapeFast and accurate mutation detection in whole genome sequences of multiple isogenic samples with IsoMutRecurrent Mutations of Chromatin-Remodeling Genes and Kinase Receptors in Pheochromocytomas and Paragangliomas.Familial adenomatous patients with desmoid tumours show increased expression of miR-34a in serum and high levels in tumours.Somatic Variants in the Human Lens Epithelium: A Preliminary Assessment.North Carolina macular dystrophy (MCDR1) caused by a novel tandem duplication of the PRDM13 gene.Epigenetic reprogramming and aberrant expression of PRAME are associated with increased metastatic risk in Class 1 and Class 2 uveal melanomas.Proteogenomic integration reveals therapeutic targets in breast cancer xenograftsGenomeVIP: a cloud platform for genomic variant discovery and interpretation.Depletion of Mouse Cells from Human Tumor Xenografts Significantly Improves Downstream Analysis of Target Cells.Standards and Guidelines for the Interpretation and Reporting of Sequence Variants in Cancer: A Joint Consensus Recommendation of the Association for Molecular Pathology, American Society of Clinical Oncology, and College of American Pathologists.Antigen presentation profiling reveals recognition of lymphoma immunoglobulin neoantigens.Novel Transcriptional Activity and Extensive Allelic Imbalance in the Human MHC Region.Germ-line and somatic EPHA2 coding variants in lens aging and cataract.DISTAG/TBCCd1 Is Required for Basal Cell Fate Determination in Ectocarpus.Slow evolution of sex-biased genes in the reproductive tissue of the dioecious plant Salix viminalis.Punctuated evolution of canonical genomic aberrations in uveal melanoma.QuantumClone: Clonal assessment of functional mutations in cancer based on a genotype-aware method for clonal reconstruction.Detection of circulating tumor DNA in patients with osteosarcoma.Sequencing of circulating tumor DNA for dynamic monitoring of gene mutations in advanced non-small cell lung cancer.Muver, a computational framework for accurately calling accumulated mutations.Exome and copy number variation analyses of Mayer-Rokitansky-Küster- Hauser syndromeGenome Wide Identification of Mutational Hotspots in the Apicomplexan Parasite Neospora caninum and the Implications for Virulence
P2860
Q35227833-2A2E357E-8375-4ED1-AB8C-AE18C06927E9Q35886692-26FC6AB0-6F34-40C4-8592-760A3CA98EE5Q36021962-6C688B38-C3C7-4FAE-8BF6-EE89DD8092E6Q36175992-26D3B1D9-0D66-44C6-9896-280FB2BCFD34Q36194303-85B8B38B-E0B9-46BA-BA42-351830B6EAB7Q36239238-2A2CE841-026A-45CF-BDDA-B6C392183700Q36265829-660B2C0F-79F5-48AF-BA10-3C463B053493Q36863246-2F72C1DC-9D58-4031-A7F5-DCE1532AA024Q37136293-01B359A6-BC82-4E9F-BB5A-0E433A19A1F0Q37179645-B22B35D5-C197-4DF3-9877-23AFD8A1D3E0Q37350839-6EEADDE3-3396-4B0B-B29B-7EAC903E0A2BQ37644842-831D72FF-F526-43AE-B405-9B9414112A5BQ37736390-C366C2BD-7A6C-4302-ADAC-76862FBBB353Q38370721-BDF18829-BEEE-496E-83AE-673C301A86F8Q38753118-67B5F201-D063-4F30-92D7-B9B6B35ADA30Q39043523-3DD92253-0E66-4D5C-BE62-BD3D65DA60D8Q46398502-386BD31D-F91D-465F-A43B-AFB5BE26BBCBQ47195282-58F66EB0-C020-4D5B-BDA6-9F08D515EA40Q47267611-3C8F86D5-1DED-438E-82BA-6F1A9A0D1A58Q47326443-E008F410-1DDC-41F5-B8C2-1B6703C52E69Q47560472-2603B722-BDCE-4C25-AC12-F22AE1ABB6B9Q48276701-79BD0129-43D1-4F1E-9733-B61CD01E27A7Q50001234-45240392-03B9-4118-A437-7EB2A3A3F697Q52725332-49E8B7A3-1052-4B0F-A80D-F01E7DC6165EQ53700833-FC6D4BC7-F4D1-4B58-906C-9129A021E3AFQ55016019-AB9B8058-163E-4690-826E-9FAE54E2876CQ57299851-DD59A48A-1C6C-4BA8-AE29-43DF3C810FF0Q58702723-60D7946E-4F22-4D80-949A-9C4F82AE6700
P2860
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
description
2013 nî lūn-bûn
@nan
2013 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@ast
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@en
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@nl
type
label
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@ast
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@en
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@nl
prefLabel
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@ast
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@en
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@nl
P2093
P2860
P1476
Using VarScan 2 for Germline Variant Calling and Somatic Mutation Detection
@en
P2093
Daniel C Koboldt
David E Larson
Richard K Wilson
P2860
P304
P356
10.1002/0471250953.BI1504S44
P577
2013-12-01T00:00:00Z