zCall: a rare variant caller for array-based genotyping: genetics and population analysis. - Wikidata - wikimedia - TriplyDB

zCall: a rare variant caller for array-based genotyping: genetics and population analysis.

zCall: a rare variant caller for array-based genotyping: genetics and population analysis.

http://www.wikidata.org/entity/Q36294014

about

Rare and low-frequency coding variants in CXCR2 and other genes are associated with hematological traits Genome sequencing elucidates Sardinian genetic architecture and augments association analyses for lipid and blood inflammatory markers Genome-Wide Association of Heroin Dependence in Han Chinese Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility A candidate gene study of capecitabine-related toxicity in colorectal cancer identifies new toxicity variants at DPYD and a putative role for ENOSF1 rather than TYMS The power of meta-analysis in genome-wide association studies Rare and low-frequency coding variants alter human adult height Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks Best practices and joint calling of the HumanExome BeadChip: the CHARGE Consortium.Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN)Quality control, imputation and analysis of genome-wide genotyping data from the Illumina HumanCoreExome microarray.Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits KRLMM: an adaptive genotype calling method for common and low frequency variants Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes.No large-effect low-frequency coding variation found for myocardial infarction Clozapine-induced agranulocytosis is associated with rare HLA-DQB1 and HLA-B alleles.Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk Predicting educational achievement from DNA.Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease.Comparison of genotype clustering tools with rare variants Illumina human exome genotyping array clustering and quality control Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs.Genome-wide burden of deleterious coding variants increased in schizophrenia.M(3)-S: a genotype calling method incorporating information from samples with known genotypes.A null mutation in ANGPTL8 does not associate with either plasma glucose or type 2 diabetes in humans Low-frequency coding variants at 6p21.33 and 20q11.21 are associated with lung cancer risk in Chinese populations Meta-GWAS and Meta-Analysis of Exome Array Studies Do Not Reveal Genetic Determinants of Serum Hepcidin.Genome-wide association analyses based on whole-genome sequencing in Sardinia provide insights into regulation of hemoglobin levels.Exome arrays capture polygenic rare variant contributions to schizophrenia.Novel Genetic Loci Associated With Retinal Microvascular Diameter Identification of type 2 diabetes subgroups through topological analysis of patient similarity.Exome-wide analysis of rare coding variation identifies novel associations with COPD and airflow limitation in MOCS3, IFIT3 and SERPINA12.Genome-wide association study of response to cognitive-behavioural therapy in children with anxiety disorders.Quality Control for the Illumina HumanExome BeadChip.Rare variants in CFI, C3 and C9 are associated with high risk of advanced age-related macular degeneration.A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolates Exome chip analyses in adult attention deficit hyperactivity disorder.Detecting large copy number variants using exome genotyping arrays in a large Swedish schizophrenia sample.Exome analysis of HIV patients submitted to dendritic cells therapeutic vaccine reveals an association of CNOT1 gene with response to the treatment.Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk.

P2860

Q28239018-C10CE8E5-E43E-423D-B40E-F2CA78564AD4 Q28267312-A5C312A6-87D3-4381-AA9B-089923AB97DB Q28554877-22EF71C4-8DE2-40D4-8031-3492F4F8E31B Q28651068-248CD932-C9BC-4D66-A2BD-C5C787EC2F6A Q28652720-367A9436-1FEA-4914-ABAF-2E28B18FA221 Q28658972-0DB7C1A1-D318-4FD7-84EE-BCE466B477E7 Q29583867-9AB1C757-5CEF-412B-93E9-C6AC2D2C1EED Q30411387-631AF3A5-E336-4D06-A744-7A1C7A30A233 Q30418185-8EA7F4C7-1412-4F83-BDB6-EC55E175C2F7 Q30458056-5FFEC2CB-5698-4104-8E8A-0D482984F0FF Q31002427-D6FC4C64-44E2-4D33-B6BE-6CA6F6D92669 Q33762970-B022D161-9630-48DB-BD78-899FE3F6FF6A Q33781868-F4726B50-5F8C-4000-B798-416B6CD84CC6 Q33921071-E24DBA58-5ED8-4A8A-B1F5-99DE1A18C2F5 Q33991765-0D78D0C8-151C-47EE-B0A3-9F6D43903C9A Q34138234-DDDB3DFD-E333-4EAE-9737-2B11EFE54FB6 Q34213805-11BAFFE3-1271-4E90-A2C8-C0DA22D7B8B5 Q34534489-D794E800-CE1E-429E-A882-729D26863B2D Q34682478-72268A36-916C-40E1-9897-EF765C656337 Q35100135-FA66C95A-2E4D-4082-93D9-20C24CFB0CEC Q35636148-B26BAD29-FFB6-42A9-85BE-A1859E26D343 Q35722160-3DF0BB6C-FB45-4727-9BB9-6FA5B6961528 Q35844617-38E86194-13FC-4B9C-9E81-9ED734802519 Q35860389-EBDFE8C7-5DD0-423A-8B98-056A364F7021 Q35907724-CE3511FD-7E55-43D8-9FD2-0ADC95F1882C Q36061600-A2B05F36-87B2-4FF5-831F-8E199867F01D Q36192873-4D8F6EFC-D661-4403-92E7-A36CFBC27182 Q36232895-3E5C520F-8B11-4C2A-B9DC-785451ABD8AC Q36581392-DDD9139B-AC4F-4763-8192-A3CD4876FAA0 Q36594014-E1F3475B-EB26-4B7A-8085-B5FBB847FAC6 Q36659399-5E4441A5-E8DB-4BCA-B2CE-B143AF6B4E4E Q36968835-A7493397-DD54-45A7-9FAB-54016FABE3A0 Q37223300-09408673-0E9B-4F5B-B3FD-A4D08E4F0572 Q37401251-C151338C-45BE-4C65-AC6D-663C19536CB9 Q37515621-97A0BA26-343D-4078-A5A6-8E4F2567D66A Q37528270-111665DC-C7F9-41E4-BDD4-7FDF97A5F1EA Q37650437-5F79CE71-14CE-45E5-A6B1-70C3264FB071 Q37663717-D4B33F10-FCEC-4FF6-847F-141D1E16DA48 Q38309700-BAF39410-40DC-4B65-A26A-36E2C7E6B519 Q38845261-26259D03-67CB-4796-A26C-11EF1C89B0AE

P2860

zCall: a rare variant caller for array-based genotyping: genetics and population analysis.

http://www.wikidata.org/entity/Q36294014

description

2012 nî lūn-bûn

@nan

2012年の論文

@ja

2012年学术文章

@wuu

2012年学术文章

@zh-cn

2012年学术文章

@zh-hans

2012年学术文章

@zh-my

2012年学术文章

@zh-sg

2012年學術文章

@yue

2012年學術文章

@zh

2012年學術文章

@zh-hant

name

zCall: a rare variant caller f ...... etics and population analysis.

@ast

zCall: a rare variant caller f ...... etics and population analysis.

@en

type

label

zCall: a rare variant caller f ...... etics and population analysis.

@ast

zCall: a rare variant caller f ...... etics and population analysis.

@en

prefLabel

zCall: a rare variant caller f ...... etics and population analysis.

@ast

zCall: a rare variant caller f ...... etics and population analysis.

@en

P1433

Q36294014-96744031-0E5E-4BE6-8627-93F3613C35F5

P1476

Q36294014-19DCCE4C-CC3B-4584-A52B-DFD597DC5253

P2093

Q36294014-0A763670-EF0C-4FC8-A7D2-6EAEB3AB1E83

Q36294014-25801392-AD12-4155-9418-AD66FFE8A6D7

Q36294014-2FB91A9C-F7C3-4C02-AEA9-47FDCD7DF2B4

Q36294014-3705845E-5090-4F87-94D3-57103BFF46F3

Q36294014-3F0CBDB0-EF27-4A6F-98C0-7F1290533E49

Q36294014-4A6D03A1-8BA1-4763-808E-93A5147EA42C

Q36294014-51123101-5B5C-420E-8C08-0217EAF0CE95

Q36294014-63EC885D-520F-4A2B-AAE7-B6710271C9A3

Q36294014-7DBBEE2F-61EB-4670-B0DE-A40F359FC776

Q36294014-892DEA66-7B43-4555-B56F-DD841C7E076C

P2860

Q36294014-1C3FD73F-5694-4656-8393-530119AAB796

Q36294014-7E9753F6-0650-4F32-A8CD-CFD32490FC6D

Q36294014-9460EE0C-F3F1-49EF-9520-F80FF70881AA

Q36294014-B84909D0-DFC5-4490-95B7-BB7B03ED694C

Q36294014-D4FD72A7-E623-457F-9BC6-B6FAA4E5A396

Q36294014-EEA261CA-25FF-42F1-AD28-CC7B08C1F92C

P304

Q36294014-2B9040D1-2446-4075-A43C-DAB7EFA40973

P31

Q36294014-D6A945DA-E00E-49D4-B384-BAABCAA914ED

P356

Q36294014-D29494E8-21B9-47B9-8BF5-7E33CC132DA6

P407

Q36294014-E4AFBDE4-688E-48D5-8365-BA94714BA9E4

P433

Q36294014-23548EF4-64EA-45E2-9A3E-36B310EE6003

P478

Q36294014-785A8DD1-F147-43F9-9502-AEFC7FF4159A

P50

Q36294014-4E123330-8087-4BE4-8FBE-97AEBD521DBC

Q36294014-5B4E8175-8778-48A0-A560-0B1455BBAB4C

Q36294014-7582F6E8-914D-4C92-BC47-456FB1825E39

Q36294014-EE18BA1D-C693-40B9-8AF0-EF4A38DD9786

P577

Q36294014-EDCCA7EF-55DF-410F-A79C-1FCB62E6B0DB

P5875

Q36294014-35370FC3-7FD8-410A-91BD-758F203C64AD

P698

Q36294014-1531F524-B713-4270-B1C6-6DCBCBC0D6C4

P932

Q36294014-BB568D99-0E97-439F-9B51-6AB18348DD1C

P356

P1433

P1476

zCall: a rare variant caller f ...... etics and population analysis.

@en

P2093

ARRA Autism Sequencing Consortium

http://www.w3.org/2001/XMLSchema#string

Andrew Crenshaw

http://www.w3.org/2001/XMLSchema#string

Benjamin M Neale

http://www.w3.org/2001/XMLSchema#string

Christine Stevens

http://www.w3.org/2001/XMLSchema#string

Colm O'Dushlaine

http://www.w3.org/2001/XMLSchema#string

George B Grant

http://www.w3.org/2001/XMLSchema#string

Jared Maguire

http://www.w3.org/2001/XMLSchema#string

Jason Carey

http://www.w3.org/2001/XMLSchema#string

Kimberly Chambert

http://www.w3.org/2001/XMLSchema#string

Menachem Fromer

http://www.w3.org/2001/XMLSchema#string

P2860

Five years of GWAS discovery

Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder

Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease

Comparing genotyping algorithms for Illumina's Infinium whole-genome SNP BeadChips.

optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants

Integrated genotype calling and association analysis of SNPs, common copy number polymorphisms and rare CNVs.

P304

2543-2545

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1093/BIOINFORMATICS/BTS479

http://www.w3.org/2001/XMLSchema#string

P407

P433

19

http://www.w3.org/2001/XMLSchema#string

P478

28

http://www.w3.org/2001/XMLSchema#string

P50

Jennifer L. Moran

Mark Joseph Daly

Jacqueline I Goldstein

Christina M. Hultman

P577

2012-07-27T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

230586319

http://www.w3.org/2001/XMLSchema#string

P698

22843986

http://www.w3.org/2001/XMLSchema#string

P932

3463112

http://www.w3.org/2001/XMLSchema#string