about
Predicting the effects of frameshifting indelsWhole-genome profiling of mutagenesis in Caenorhabditis elegansComputational and bioinformatics frameworks for next-generation whole exome and genome sequencingIntegrating Epigenomics into the Understanding of Biomedical InsightPhenotypic and genome-wide analysis of an antibiotic-resistant small colony variant (SCV) of Pseudomonas aeruginosaGenome analysis of a transmissible lineage of pseudomonas aeruginosa reveals pathoadaptive mutations and distinct evolutionary paths of hypermutatorsAre differences in genomic data sets due to true biological variants or errors in genome assembly: an example from two chloroplast genomesCharacterization of genetic diversity in the nematode Pristionchus pacificus from population-scale resequencing dataComparison of insertion/deletion calling algorithms on human next-generation sequencing data.Performance evaluation of indel calling tools using real short-read dataUsing high-throughput sequencing transcriptome data for INDEL detection: challenges for cancer drug discovery.The characterization of twenty sequenced human genomes.Human metapneumovirus infection induces significant changes in small noncoding RNA expression in airway epithelial cells.Dindel: accurate indel calls from short-read data.Discovery of genome-wide DNA polymorphisms in a landrace cultivar of Japonica rice by whole-genome sequencing.A probabilistic method for the detection and genotyping of small indels from population-scale sequence data.Whole-exome sequencing of DNA from peripheral blood mononuclear cells (PBMC) and EBV-transformed lymphocytes from the same donorTri6 is a global transcription regulator in the phytopathogen Fusarium graminearum.The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process.Detecting genomic indel variants with exact breakpoints in single- and paired-end sequencing data using SplazerS.Discovery of novel variants in genotyping arrays improves genotype retention and reduces ascertainment bias.Analysis of insertion-deletion from deep-sequencing data: software evaluation for optimal detection.Characterisation and validation of insertions and deletions in 173 patient exomesA survey of sequence alignment algorithms for next-generation sequencing.Equivalent indels--ambiguous functional classes and redundancy in databases.Genome-wide DNA polymorphisms in two cultivars of mei (Prunus mume sieb. et zucc.).The venom gland transcriptome of Latrodectus tredecimguttatus revealed by deep sequencing and cDNA library analysis.Coexistence and within-host evolution of diversified lineages of hypermutable Pseudomonas aeruginosa in long-term cystic fibrosis infections.Detection and characterization of small insertion and deletion genetic variants in modern layer chicken genomes.Improving RNA-Seq Precision with MapAl.The missing indels: an estimate of indel variation in a human genome and analysis of factors that impede detection.FANSe: an accurate algorithm for quantitative mapping of large scale sequencing reads.Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation.Is genotyping of single isolates sufficient for population structure analysis of Pseudomonas aeruginosa in cystic fibrosis airways?Estimating error models for whole genome sequencing using mixtures of Dirichlet-multinomial distributions.An oxidative DNA "damage" and repair mechanism localized in the VEGF promoter is important for hypoxia-induced VEGF mRNA expression.Loss-of-function mutations in the IL-21 receptor gene cause a primary immunodeficiency syndromeComparative genomic analysis of rapid evolution of an extreme-drug-resistant Acinetobacter baumannii cloneThe landscape of microsatellite instability in colorectal and endometrial cancer genomes.Next-generation carrier screening
P2860
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P2860
description
2010 nî lūn-bûn
@nan
2010 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Microindel detection in short-read sequence data.
@ast
Microindel detection in short-read sequence data.
@en
Microindel detection in short-read sequence data.
@nl
type
label
Microindel detection in short-read sequence data.
@ast
Microindel detection in short-read sequence data.
@en
Microindel detection in short-read sequence data.
@nl
prefLabel
Microindel detection in short-read sequence data.
@ast
Microindel detection in short-read sequence data.
@en
Microindel detection in short-read sequence data.
@nl
P2093
P2860
P50
P356
P1433
P1476
Microindel detection in short-read sequence data.
@en
P2093
Christian Rödelsperger
Luke Jostins
Marten Jäger
Sebastian Bauer
P2860
P304
P356
10.1093/BIOINFORMATICS/BTQ027
P407
P577
2010-02-09T00:00:00Z