Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
about
Interpreting whole genome sequencing for investigating tuberculosis transmission: a systematic review.Three-stage quality control strategies for DNA re-sequencing dataThe de novo genome assembly and annotation of a female domestic dromedary of North African originImpacts of low coverage depths and post-mortem DNA damage on variant calling: a simulation studyMolecular diagnosis of autosomal dominant polycystic kidney disease using next-generation sequencing.An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.Coval: improving alignment quality and variant calling accuracy for next-generation sequencing data.Non-synonymous variations in cancer and their effects on the human proteome: workflow for NGS data biocuration and proteome-wide analysis of TCGA data.Choice of reference sequence and assembler for alignment of Listeria monocytogenes short-read sequence data greatly influences rates of error in SNP analyses.Review of current methods, applications, and data management for the bioinformatics analysis of whole exome sequencing.Evaluation of variant identification methods for whole genome sequencing data in dairy cattle.Masking as an effective quality control method for next-generation sequencing data analysis.Next Generation Semiconductor Based Sequencing of the Donkey (Equus asinus) Genome Provided Comparative Sequence Data against the Horse Genome and a Few Millions of Single Nucleotide PolymorphismsChoice of reference-guided sequence assembler and SNP caller for analysis of Listeria monocytogenes short-read sequence data greatly influences rates of error.Evaluating the necessity of PCR duplicate removal from next-generation sequencing data and a comparison of approachesAnalysis of single nucleotide polymorphisms based on RNA sequencing data of diverse bio-geographical accessions in barley.Multi-perspective quality control of Illumina RNA sequencing data analysis.Impact of post-alignment processing in variant discovery from whole exome dataGenetic insights into juvenile idiopathic arthritis derived from deep whole genome sequencing.A reference human genome dataset of the BGISEQ-500 sequencer.High proportion of heteroresistance in gyrA and gyrB in fluoroquinolone-resistant Mycobacterium tuberculosis clinical isolatesDesign and development of exome capture sequencing for the domestic pig (Sus scrofa).Validation and assessment of variant calling pipelines for next-generation sequencing.Targeted exon sequencing fails to identify rare coding variants with large effect in rheumatoid arthritisNext-generation sequencing in clinical oncology: next steps towards clinical validationTargeted Sequencing Reveals Large-Scale Sequence Polymorphism in Maize Candidate Genes for Biomass Production and Composition.A Retrospective Study on Genetic Heterogeneity within Treponema Strains: Subpopulations Are Genetically Distinct in a Limited Number of Positions.Trimming of sequence reads alters RNA-Seq gene expression estimates.Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study.Phylogenomic Insights into Mouse Evolution Using a Pseudoreference Approach.REPURPOSING GERMLINE EXOMES OF THE CANCER GENOME ATLAS DEMANDS A CAUTIOUS APPROACH AND SAMPLE-SPECIFIC VARIANT FILTERINGNext generation sequencing in cancer research and clinical applicationA hybrid computational strategy to address WGS variant analysis in >5000 samples.Red-legged partridge (Alectoris rufa) de-novo transcriptome assembly and identification of gene-related markers.A Primer on Infectious Disease Bacterial GenomicsComparative study of whole genome amplification and next generation sequencing performance of single cancer cells.Genomics in 2012: challenges and opportunities in the next generation sequencing era.Development and Applications of a High Throughput Genotyping Tool for Polyploid Crops: Single Nucleotide Polymorphism (SNP) Array.Tobacco habituated and non-habituated subjects exhibit different mutational spectrums in head and neck squamous cell carcinoma.RNA variant identification discrepancy among splice-aware alignment algorithms
P2860
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P2860
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
description
2012 nî lūn-bûn
@nan
2012 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2012年の論文
@ja
2012年論文
@yue
2012年論文
@zh-hant
2012年論文
@zh-hk
2012年論文
@zh-mo
2012年論文
@zh-tw
2012年论文
@wuu
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Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
@ast
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
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type
label
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
@ast
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
@en
prefLabel
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
@ast
Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
@en
P2093
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Steps to ensure accuracy in genotype and SNP calling from Illumina sequencing data.
@en
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P356
10.1186/1471-2164-13-S8-S8
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P478
13 Suppl 8
P577
2012-12-17T00:00:00Z
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1015629824