About: Aaron R Quinlan

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher

Attributes	Values
rdf:type	Item
description	forskare (sv) researcher (en) 연구원 (ko) ricercatore (it) গবেষক (bn) 研究者 (ja) investigador (es) chercheur (fr) wetenschapper (nl) дослідник (uk) वैज्ञानिक (hi) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (en-ca) researcher (en-gb) researcher (en-us) investigador (ca) investigador (gl) investigador (ast) investigador (pt)
exact match	wds:Q37392647-D6F0AFA9-D0EC-4380-A826-C4D05FD8BC3B
exact match	https://scigraph.springernature.com/person.0612231705.45
rdfs:label	Aaron R Quinlan (en) Aaron R Quinlan (es) Aaron R Quinlan (nl) Aaron R Quinlan (sl) Aaron R Quinlan (ast) Aaron R. Quinlan (it)
skos:prefLabel	Aaron R Quinlan (en) Aaron R Quinlan (es) Aaron R Quinlan (nl) Aaron R Quinlan (sl) Aaron R Quinlan (ast) Aaron R. Quinlan (it)
name	Aaron R Quinlan (en) Aaron R Quinlan (es) Aaron R Quinlan (nl) Aaron R Quinlan (sl) Aaron R Quinlan (ast) Aaron R. Quinlan (it)
given name	wds:Q37392647-6E1DA19F-C48C-4F49-A05A-0FF2CEA944E5
given name	Aaron
instance of	wds:Q37392647-C33FCCD4-2077-4CA2-BB6C-7C428EECD8E5
instance of	Homo sapiens
skos:altLabel	Aaron Quinlan (en)
occupation	wds:Q37392647-EEFF7D82-4E2F-482F-A495-FE38BBDB47CE
sex or gender	wds:Q37392647-9C9AF53F-40B2-411E-9D5C-0996C247DB7C
DBLP author ID	wds:Q37392647-4C93E91E-E5AD-4F1C-B802-44AB8AE9EE1F
educated at	wds:Q37392647-E6B4B8CE-EA55-4695-AB60-5C56981732B1
DBLP author ID	https://dblp.org/pid/84/7969.rdf
occupation	researcher
sex or gender	male
DBLP author ID	84/7969
educated at	College of William & Mary
ORCID iD	wds:Q37392647-4A35FDB7-0896-48CC-BBF4-E39FA2A36327
Dimensions author ID	wds:Q37392647-297A2293-4ACE-4D26-8818-73648E65D65C
ORCID iD	https://orcid.org/0000-0003-1756-0859
ORCID iD	0000-0003-1756-0859
Dimensions author ID	0612231705.45
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q37392647
is author of	BEDTools: a flexible suite of utilities for comparing genomic features Genome-wide mapping and assembly of structural variant breakpoints in the mouse genome Pyrobayes: an improved base caller for SNP discovery in pyrosequences. Population genomic inferences from sparse high-throughput sequencing of two populations of Drosophila melanogaster Characterizing complex structural variation in germline and somatic genomes Genetics of systemic lupus erythematosus: immune responses and end organ resistance to damage GEMINI: integrative exploration of genetic variation and genome annotations Copy number variation detection and genotyping from exome sequence data Efficient genotype compression and analysis of large genetic-variation data sets. Evidence for two independent associations with type 1 diabetes at the 12q13 locus Breakpoint profiling of 64 cancer genomes reveals numerous complex rearrangements spawned by homology-independent mechanisms Pybedtools: a flexible Python library for manipulating genomic datasets and annotations Whole-genome sequencing and variant discovery in C. elegans. A reference bacterial genome dataset generated on the MinION™ portable single-molecule nanopore sequencer. Rapid whole-genome mutational profiling using next-generation sequencing technologies Genome sequencing of mouse induced pluripotent stem cells reveals retroelement stability and infrequent DNA rearrangement during reprogramming LUMPY: a probabilistic framework for structural variant discovery. Binary Interval Search: a scalable algorithm for counting interval intersections Poretools: a toolkit for analyzing nanopore sequence data Primer-site SNPs mask mutations. Cas9-chromatin binding information enables more accurate CRISPR off-target prediction. BamTools: a C++ API and toolkit for analyzing and managing BAM files BEDTools: The Swiss-Army Tool for Genome Feature Analysis. Rare and Coding Region Genetic Variants Associated With Risk of Ischemic Stroke: The NHLBI Exome Sequence Project SubcloneSeeker: a computational framework for reconstructing tumor clone structure for cancer variant interpretation and prioritization Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers Who's Who? Detecting and Resolving Sample Anomalies in Human DNA Sequencing Studies with Peddy mosdepth: quick coverage calculation for genomes and exomes Indexcov: fast coverage quality control for whole-genome sequencing A novel IFITM5 mutation in severe atypical osteogenesis imperfecta type VI impairs osteoblast production of pigment epithelium-derived factor Erratum: A reference bacterial genome dataset generated on the MinION(TM) portable single-molecule nanopore sequencer Extending reference assembly models Homozygous mutation of MTPAP causes cellular radiosensitivity and persistent DNA double-strand breaks SpeedSeq: ultra-fast personal genome analysis and interpretation Nanopore sequencing and assembly of a human genome with ultra-long reads. Targeted Deep Sequencing in Multiple-Affected Sibships of European Ancestry Identifies Rare Deleterious Variants in PTPN22 That Confer Risk for Type 1 Diabetes Detection and interpretation of genomic structural variation in mammals

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