An initial map of insertion and deletion (INDEL) variation in the human genome. - Wikidata - awgldk - TriplyDB

An initial map of insertion and deletion (INDEL) variation in the human genome.

An initial map of insertion and deletion (INDEL) variation in the human genome.

http://www.wikidata.org/entity/Q33998460

about

The diploid genome sequence of an individual human Genetic variation in healthy oldest-old U87MG decoded: the genomic sequence of a cytogenetically aberrant human cancer cell line Genetic variation in an individual human exome Predicting the effects of frameshifting indels Towards a comprehensive structural variation map of an individual human genome Characterization and potential functional significance of human-chimpanzee large INDEL variation Human genetics and genomics a decade after the release of the draft sequence of the human genome Insertion-deletion polymorphisms (indels) as genetic markers in natural populations Using ERDS to infer copy-number variants in high-coverage genomes Mapping copy number variation by population-scale genome sequencing A map of human genome variation from population-scale sequencing Nucleotide-resolution analysis of structural variants using BreakSeq and a breakpoint library Ultraconserved elements: analyses of dosage sensitivity, motifs and boundaries Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding Mechanisms underlying structural variant formation in genomic disorders Different Facets of Copy Number Changes: Permanent, Transient, and Adaptive Detection of Genomic Structural Variants from Next-Generation Sequencing Data Exploring the role of copy number variants in human adaptation CNVnator: an approach to discover, genotype, and characterize typical and atypical CNVs from family and population genome sequencing A genome-wide approach for detecting novel insertion-deletion variants of mid-range size Genetic variation in the proximal promoter of ABC and SLC superfamilies: liver and kidney specific expression and promoter activity predict variation Lineage-specific genomics: Frequent birth and death in the human genome: The human genome contains many lineage-specific elements created by both sequence and functional turnover Gene inactivation and its implications for annotation in the era of personal genomics The population genetics of structural variation PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads Natural mutagenesis of human genomes by endogenous retrotransposons Meet me halfway: when genomics meets structural bioinformatics.Characterizing complex structural variation in germline and somatic genomes Residue mutations and their impact on protein structure and function: detecting beneficial and pathogenic changes.DDIG-in: discriminating between disease-associated and neutral non-frameshifting micro-indels Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome Human genes involved in copy number variation: mechanisms of origin, functional effects and implications for disease.A population model for genotyping indels from next-generation sequence data.PyroHMMvar: a sensitive and accurate method to call short indels and SNPs for Ion Torrent and 454 data.iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data Population genetic data and forensic parameters of 30 autosomal InDel markers in Santa Catarina State population, Southern Brazil.Reducing INDEL calling errors in whole genome and exome sequencing data.

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P2860

An initial map of insertion and deletion (INDEL) variation in the human genome.

http://www.wikidata.org/entity/Q33998460

description

2006 nî lūn-bûn

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2006 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի օգոստոսին հրատարակված գիտական հոդված

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2006年の論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年論文

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2006年论文

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name

An initial map of insertion and deletion (INDEL) variation in the human genome.

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An initial map of insertion and deletion (INDEL) variation in the human genome.

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type

label

An initial map of insertion and deletion (INDEL) variation in the human genome.

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An initial map of insertion and deletion (INDEL) variation in the human genome.

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prefLabel

An initial map of insertion and deletion (INDEL) variation in the human genome.

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An initial map of insertion and deletion (INDEL) variation in the human genome.

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Genome Research

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An initial map of insertion and deletion (INDEL) variation in the human genome

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Adam Beauchamp

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Christine E Larkins

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Christopher T Luttig

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Circe Tsui

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Scott E Devine

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W Stephen Pittard

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P2860

The human genome browser at UCSC

A haplotype map of the human genome

Statistical significance for genomewide studies

The structure of haplotype blocks in the human genome

Base-calling of automated sequencer traces using phred. II. Error probabilities

The International HapMap Project

A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms

A DNA polymorphism discovery resource for research on human genetic variation

Repbase update: a database and an electronic journal of repetitive elements

Recent segmental duplications in the human genome

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10.1101/GR.4565806

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9

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