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GIBBS, RICHARD

One or more keywords matched the following items that are connected to GIBBS, RICHARD

Item Type	Name
Academic Article	SNPdetector: a software tool for sensitive and accurate SNP detection.
Academic Article	The Atlas genome assembly system.
Academic Article	The complete genome of an individual by massively parallel DNA sequencing.
Academic Article	Identification of rat genes by TWINSCAN gene prediction, RT-PCR, and direct sequencing.
Academic Article	An integrative variant analysis suite for whole exome next-generation sequencing data.
Academic Article	CGAP-align: a high performance DNA short read alignment tool.
Academic Article	Dynamic building of a BAC clone tiling path for the Rat Genome Sequencing Project.
Academic Article	Minimum information about a marker gene sequence (MIMARKS) and minimum information about any (x) sequence (MIxS) specifications.
Academic Article	Mind the gap: upgrading genomes with Pacific Biosciences RS long-read sequencing technology.
Academic Article	Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls.
Concept	Software
Academic Article	Launching genomics into the cloud: deployment of Mercury, a next generation sequence analysis pipeline.
Academic Article	Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.
Academic Article	Assessing structural variation in a personal genome-towards a human reference diploid genome.
Academic Article	The Matchmaker Exchange: a platform for rare disease gene discovery.
Academic Article	WGSA: an annotation pipeline for human genome sequencing studies.
Academic Article	DNAism: exploring genomic datasets on the web with Horizon Charts.
Academic Article	SeqCNV: a novel method for identification of copy number variations in targeted next-generation sequencing data.
Academic Article	Exome sequencing reveals novel genetic loci influencing obesity-related traits in Hispanic children.
Academic Article	Analysis commons, a team approach to discovery in a big-data environment for genetic epidemiology.
Grant	Draft Sequence of the Rat Genome
Grant	Filling the data processing gap for exon-region specific data from 1000 Genomes
Grant	MEGABASE SEQUENCING OF HUMAN XQ28
Grant	The Baylor-Hopkins Clinical Genomics Center for All of Us
Academic Article	Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel.
Academic Article	Evaluation of computational genotyping of structural variation for clinical diagnoses.
Academic Article	Parliament2: Accurate structural variant calling at scale.
Academic Article	Neptune: an environment for the delivery of genomic medicine.

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Software