about
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot projectThe GENCODE pseudogene resourceIdentification and analysis of unitary pseudogenes: historic and contemporary gene losses in humans and other primatesGENCODE: producing a reference annotation for ENCODEEGASP: the human ENCODE Genome Annotation Assessment ProjectEvidence for transcript networks composed of chimeric RNAs in human cellsA conditional knockout resource for the genome-wide study of mouse gene functionPseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolutionEnsembl 2014The GENCODE v7 catalog of human long noncoding RNAs: analysis of their gene structure, evolution, and expressionGENCODE: the reference human genome annotation for The ENCODE ProjectThe importance of identifying alternative splicing in vertebrate genome annotationTracking and coordinating an international curation effort for the CCDS ProjectThe consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomesDNA sequence of human chromosome 17 and analysis of rearrangement in the human lineageProminent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regionsAnnoTrack - a tracking system for genome annotationMultiple evidence strands suggest that there may be as few as 19,000 human protein-coding genesEnsembl 2012Ensembl 2013Comparative analysis of pseudogenes across three phylaGene inactivation and its implications for annotation in the era of personal genomicsThe implications of alternative splicing in the ENCODE protein complementDetermination and validation of principal gene products.Systematic evaluation of spliced alignment programs for RNA-seq dataEfficient targeted transcript discovery via array-based normalization of RACE libraries.MHC-linked and un-linked class I genes in the wallaby.Discovery of candidate disease genes in ENU-induced mouse mutants by large-scale sequencing, including a splice-site mutation in nucleoredoxin.Genome annotation for clinical genomic diagnostics: strengths and weaknessesTranscriptome analysis of human tissues and cell lines reveals one dominant transcript per geneMeeting report: a workshop on Best Practices in Genome Annotation.Genome-wide association meta-analysis of human longevity identifies a novel locus conferring survival beyond 90 years of age.The tammar wallaby major histocompatibility complex shows evidence of past genomic instability.Shotgun proteomics aids discovery of novel protein-coding genes, alternative splicing, and "resurrected" pseudogenes in the mouse genomeAssessment of transcript reconstruction methods for RNA-seq.Improving GENCODE reference gene annotation using a high-stringency proteogenomics workflow.Extension of human lncRNA transcripts by RACE coupled with long-read high-throughput sequencing (RACE-Seq).Genomic anatomy of the Tyrp1 (brown) deletion complex.The origins, evolution, and functional potential of alternative splicing in vertebrates.Performance assessment of promoter predictions on ENCODE regions in the EGASP experiment.
P50
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P50
description
hulumtuese
@sq
onderzoeker
@nl
researcher
@en
հետազոտող
@hy
name
Jennifer Harrow
@ast
Jennifer Harrow
@en
Jennifer Harrow
@es
Jennifer Harrow
@nl
Jennifer Harrow
@sl
type
label
Jennifer Harrow
@ast
Jennifer Harrow
@en
Jennifer Harrow
@es
Jennifer Harrow
@nl
Jennifer Harrow
@sl
prefLabel
Jennifer Harrow
@ast
Jennifer Harrow
@en
Jennifer Harrow
@es
Jennifer Harrow
@nl
Jennifer Harrow
@sl