about
Major Improvements to the Heliconius melpomene Genome Assembly Used to Confirm 10 Chromosome Fusion Events in 6 Million Years of Butterfly Evolution.Omics-Based Strategies in Precision Medicine: Toward a Paradigm Shift in Inborn Errors of Metabolism InvestigationsChallenges of Identifying Clinically Actionable Genetic Variants for Precision MedicineEnsembl core software resources: storage and programmatic access for DNA sequence and genome annotationBig Data Analytics for Genomic MedicineBiological data sciences in genome research.The Genomic Scrapheap Challenge; Extracting Relevant Data from Unmapped Whole Genome Sequencing Reads, Including Strain Specific Genomic Segments, in Rats.Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomesGenome graphs and the evolution of genome inferenceEvaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assemblyPhased diploid genome assembly with single-molecule real-time sequencing.Whole genome sequences are required to fully resolve the linkage disequilibrium structure of human populationsA unified gene catalog for the laboratory mouse reference genome.NGSmethDB 2017: enhanced methylomes and differential methylationInformatics resources for the Collaborative Cross and related mouse populationsIdentification of Candidate Functional Elements in the Genome from ChIP-seq Data.Coordinates and intervals in graph-based reference genomesDefining KIR and HLA Class I Genotypes at Highest Resolution via High-Throughput Sequencing.Discrepancies between human DNA, mRNA and protein reference sequences and their relation to single nucleotide variants in the human population.Alternate-locus aware variant calling in whole genome sequencing.Reference standards for next-generation sequencing.Recent advances in ChIP-seq analysis: from quality management to whole-genome annotation.Principles and Recommendations for Standardizing the Use of the Next-Generation Sequencing Variant File in Clinical Settings.Highly Variable Genomic Landscape of Endogenous Retroviruses in the C57BL/6J Inbred Strain, Depending on Individual Mouse, Gender, Organ Type, and Organ Location.Discovery and genotyping of novel sequence insertions in many sequenced individuals.Mapping and phasing of structural variation in patient genomes using nanopore sequencing.Detection of long repeat expansions from PCR-free whole-genome sequence data.Graphtyper enables population-scale genotyping using pangenome graphs.Analysis and Annotation of Whole-Genome or Whole-Exome Sequencing Derived Variants for Clinical Diagnosis.GenomeLandscaper: Landscape analysis of genome-fingerprints maps assessing chromosome architecture.Kourami: graph-guided assembly for novel human leukocyte antigen allele discovery.Settling the score: variant prioritization and Mendelian disease.Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects
P2860
Q27347601-D59C9FC3-DA9E-4798-BBAB-FBFCC1C8EE84Q28068009-F837CF2A-AB42-49A3-B191-91D13091A752Q28596030-C1A05225-E28C-4DE9-985F-2DD14F2B8173Q28976383-408FACC1-AE8B-4854-ABC4-45595D762AE3Q30235891-7EC35822-4579-4969-A8C3-0396B7975036Q31000649-39649092-DA9C-41AE-BDD4-4DB9A0EEFD4FQ31120231-0CE62B2D-E612-4974-8837-0FDF1EF1991FQ31149639-1D59B4B8-0FAE-4E15-9526-880623E0F66AQ33622582-DEEA2A6C-8900-4C39-B6C1-B69BA16E1E10Q33622610-BDF3A53A-996F-4421-A15D-3C6757F20719Q33887832-C7BDE41A-9BD6-48BC-BF75-83E8A99B579AQ35763565-580C5D11-E3FD-4E81-B859-4D011BF5ED8BQ35946909-B8079391-5A3B-4E5D-92BD-D2FE7D73197BQ36177822-9494CBAC-000D-4362-BA2D-88129FEA95A0Q36248743-C3788261-EE34-440A-8347-AF67846A9CA6Q36325007-75E908F0-C558-47D5-A706-D1D0FC0A2547Q36375902-7587BCD9-1E59-4C8B-96A3-4A625315A0B9Q37153103-B39761B9-E25F-42BC-BF35-AE8D937B2B08Q37227813-E1E0577A-56C9-4518-9C21-F7716581CA41Q37501768-7EA35045-6A8C-42C8-8F7D-89032DB57420Q38669617-07AB93F9-AF78-48E2-85C2-9C8D7F63E62AQ38775774-DEB148EE-F7E9-4750-87FC-7F0293959DF3Q38896358-3D849C8E-20CB-4D46-8A09-BDFCDF545936Q41688892-D11B36AB-B8F7-4282-8354-7CA23A206905Q42697230-05E32240-1CE3-4246-A249-0FDB4AB82DB4Q44794525-4EA68C02-F69B-48DC-A7EC-F9086D61D4F5Q46065898-C3412182-1AF2-46CA-B302-C7193DF5F401Q47637069-BC90A8D1-0476-4F19-B07E-C0C89AE64073Q47770082-D1E6E2A0-5162-44ED-8B6B-570111414AB6Q48215483-FF4CD3C8-D9A7-4CD3-BEE7-F1BC87D4D60CQ50130961-174F5EDF-79FC-4AC8-880B-9A5B33794474Q52544730-F88BD6CC-E6E0-4D37-88F0-D79DD659FC79Q57048739-6F4C96BA-5E93-48F7-A725-8BE3E485772E
P2860
description
2015 nî lūn-bûn
@nan
2015 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
Extending reference assembly models.
@ast
Extending reference assembly models.
@en
type
label
Extending reference assembly models.
@ast
Extending reference assembly models.
@en
prefLabel
Extending reference assembly models.
@ast
Extending reference assembly models.
@en
P2093
P2860
P50
P1433
P1476
Extending reference assembly models.
@en
P2093
Deanna M Church
Gabor T Marth
M Lisandra Zepeda Mendoza
Paul A Kitts
Valerie A Schneider
P2860
P2888
P356
10.1186/S13059-015-0587-3
P50
P577
2015-01-24T00:00:00Z