about
Three-stage quality control strategies for DNA re-sequencing dataWhole genome sequencing of field isolates provides robust characterization of genetic diversity in Plasmodium vivaxDisentangling genetic and epigenetic determinants of ultrafast adaptationA novel MC1R allele for black coat colour reveals the Polynesian ancestry and hybridization patterns of Hawaiian feral pigsA program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3Mutations in SH3PXD2B cause Borrone dermato-cardio-skeletal syndrome.Validation of Next-Generation Sequencing of Entire Mitochondrial Genomes and the Diversity of Mitochondrial DNA Mutations in Oral Squamous Cell Carcinoma.Identification of somatic mutations in cancer through Bayesian-based analysis of sequenced genome pairsReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data.PyroHMMsnp: an SNP caller for Ion Torrent and 454 sequencing data.PyroHMMvar: a sensitive and accurate method to call short indels and SNPs for Ion Torrent and 454 data.VarBin, a novel method for classifying true and false positive variants in NGS data.ANGSD: Analysis of Next Generation Sequencing Data.mtDNA-Server: next-generation sequencing data analysis of human mitochondrial DNA in the cloudImpact of post-alignment processing in variant discovery from whole exome dataFrom next-generation resequencing reads to a high-quality variant data set.Systematic identification and characterization of RNA editing in prostate tumors.Sequencing studies in human genetics: design and interpretation.A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data.Evaluation of exome sequencing to estimate tumor burden in plasma.Global assessment of genomic variation in cattle by genome resequencing and high-throughput genotyping.Analysis of high-depth sequence data for studying viral diversity: a comparison of next generation sequencing platforms using Segminator II.Heterogeneity in the inter-tumor transcriptome of high risk prostate cancer.Mutations in the mechanotransduction protein PIEZO1 are associated with hereditary xerocytosis.Consensus rules in variant detection from next-generation sequencing dataJoint genotype calling with array and sequence data.Confidence-based somatic mutation evaluation and prioritizationThe social brain: transcriptome assembly and characterization of the hippocampus from a social subterranean rodent, the colonial tuco-tuco (Ctenomys sociabilis)RADIA: RNA and DNA integrated analysis for somatic mutation detection.An integrative variant analysis pipeline for accurate genotype/haplotype inference in population NGS dataIdentification of a nonsense mutation in CWC15 associated with decreased reproductive efficiency in Jersey cattleComprehensive variation discovery in single human genomes.RNA-Seq effectively monitors gene expression in Eutrema salsugineum plants growing in an extreme natural habitat and in controlled growth cabinet conditions.Comparing variant calling algorithms for target-exon sequencing in a large sampleClinSeK: a targeted variant characterization framework for clinical sequencing.Reducing amplification artifacts in high multiplex amplicon sequencing by using molecular barcodes.Using Drosophila melanogaster as a Model for Genotoxic Chemical Mutational Studies with a New Program, SnpSiftHIV-1 Promoter Single Nucleotide Polymorphisms Are Associated with Clinical Disease SeverityMutations in the Gardos channel (KCNN4) are associated with hereditary xerocytosis.SNVSniffer: an integrated caller for germline and somatic single-nucleotide and indel mutations.
P2860
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P2860
description
2011 nî lūn-bûn
@nan
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
2011年论文
@zh
2011年论文
@zh-cn
name
Improving SNP discovery by base alignment quality.
@en
type
label
Improving SNP discovery by base alignment quality.
@en
altLabel
Improving SNP discovery by base alignment quality
@en
prefLabel
Improving SNP discovery by base alignment quality.
@en
P2860
P356
P1433
P1476
Improving SNP discovery by base alignment quality.
@en
P2860
P304
P356
10.1093/BIOINFORMATICS/BTR076
P407
P50
P577
2011-02-13T00:00:00Z