Mapping short DNA sequencing reads and calling variants using mapping quality scores
about
The date of interbreeding between Neandertals and modern humansDouble digest RADseq: an inexpensive method for de novo SNP discovery and genotyping in model and non-model speciesChromatin landscape dictates HSF binding to target DNA elementsMetabolic reconstruction for metagenomic data and its application to the human microbiomeArioc: high-throughput read alignment with GPU-accelerated exploration of the seed-and-extend search spaceEarly Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical PatientA complete mitochondrial genome sequence from a mesolithic wild aurochs (Bos primigenius)BFAST: an alignment tool for large scale genome resequencingWhole genome amplification and de novo assembly of single bacterial cells.A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogsU87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell lineGene gain and loss during evolution of obligate parasitism in the white rust pathogen of Arabidopsis thalianaDe novo genome sequence assembly of a filamentous fungus using Sanger, 454 and Illumina sequence dataUltrafast and memory-efficient alignment of short DNA sequences to the human genomeEnrichment of sequencing targets from the human genome by solution hybridizationA comparative analysis of exome captureDNA methylation patterns associate with genetic and gene expression variation in HapMap cell linesEvolution of an adenocarcinoma in response to selection by targeted kinase inhibitorsDesigning Efficient Spaced Seeds for SOLiD Read MappingFast identification and removal of sequence contamination from genomic and metagenomic datasetsUnlocking short read sequencing for metagenomicsOngoing phenotypic and genomic changes in experimental coevolution of RNA bacteriophage Qβ and Escherichia coliPractical guidelines for the comprehensive analysis of ChIP-seq dataFast mapping of short sequences with mismatches, insertions and deletions using index structuresPersonal genome sequencing: current approaches and challengesGenetic diagnosis by whole exome capture and massively parallel DNA sequencingExperimental selection of hypoxia-tolerant Drosophila melanogasterSequencing pools of individuals — mining genome-wide polymorphism data without big fundingRepetitive DNA and next-generation sequencing: computational challenges and solutionsAscaris suum draft genomeComplete Khoisan and Bantu genomes from southern Africa.Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformationsMutations in ABCD4 cause a new inborn error of vitamin B12 metabolismA form of the metabolic syndrome associated with mutations in DYRK1BThe essential role of centrosomal NDE1 in human cerebral cortex neurogenesisHomozygosity mapping and exome sequencing reveal GATAD1 mutation in autosomal recessive dilated cardiomyopathyAnalysis of the small RNA transcriptional response in multidrug-resistant Staphylococcus aureus after antimicrobial exposureRNA-Seq: a revolutionary tool for transcriptomicsWhole-genome profiling of mutagenesis in Caenorhabditis elegansMetagenomic microbial community profiling using unique clade-specific marker genes
P2860
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P2860
Mapping short DNA sequencing reads and calling variants using mapping quality scores
description
2008 nî lūn-bûn
@nan
2008 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@ast
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@en
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@nl
type
label
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@ast
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@en
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@nl
prefLabel
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@ast
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@en
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@nl
P2860
P3181
P356
P1433
P1476
Mapping short DNA sequencing reads and calling variants using mapping quality scores
@en
P2093
P2860
P304
P3181
P356
10.1101/GR.078212.108
P407
P577
2008-11-01T00:00:00Z