The Sorcerer II Global Ocean Sampling expedition: expanding the universe of protein familiesThe diploid genome sequence of an individual humanEvaluation of paired-end sequencing strategies for detection of genome rearrangements in cancerExperimental selection of hypoxia-tolerant Drosophila melanogasterHuman beta-defensin 2 is a salt-sensitive peptide antibiotic expressed in human lungCombinatorics of the breakage-fusion-bridge mechanismWhole-genome sequencing uncovers the genetic basis of chronic mountain sickness in Andean highlandersSequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encodingComparative proteogenomics: combining mass spectrometry and comparative genomics to analyze multiple genomesWhole proteome analysis of post-translational modifications: applications of mass-spectrometry for proteogenomic annotationThe genetic basis of chronic mountain sicknessAutomated querying and identification of novel peptides using MALDI mass spectrometric imagingHaplotyping as perfect phylogeny: a direct approachPredicting Carriers of Ongoing Selective Sweeps without Knowledge of the Favored AlleleiDASH: integrating data for analysis, anonymization, and sharingCompressing genomic sequence fragments using SlimGeneNext-Generation Sequencing of Plasmodium vivax Patient Samples Shows Evidence of Direct Evolution in Drug-Resistance Genes.De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly.Proteogenomic database construction driven from large scale RNA-seq data.SCOPE: a probabilistic model for scoring tandem mass spectra against a peptide database.Inferring gene ontologies from pairwise similarity data.Proteogenomic strategies for identification of aberrant cancer peptides using large-scale next-generation sequencing data.Evidence for large inversion polymorphisms in the human genome from HapMap dataAn MCMC algorithm for haplotype assembly from whole-genome sequence dataInference about recombination from haplotype data: lower bounds and recombination hotspots.TCLUST: a fast method for clustering genome-scale expression data.Designing deep sequencing experiments: detecting structural variation and estimating transcript abundanceConstruction of a medicinal leech transcriptome database and its application to the identification of leech homologs of neural and innate immune genes.A covering method for detecting genetic associations between rare variants and common phenotypes.Virmid: accurate detection of somatic mutations with sample impurity inferenceWhole genome sequencing of Ethiopian highlanders reveals conserved hypoxia tolerance genesExpansion of the mycobacterial "PUPylome"Resurrection of a clinical antibody: template proteogenomic de novo proteomic sequencing and reverse engineering of an anti-lymphotoxin-α antibody.Sensitive gene fusion detection using ambiguously mapping RNA-Seq read pairs.Strobe sequence design for haplotype assembly.Clear: Composition of Likelihoods for Evolve and Resequence Experiments.Template proteogenomics: sequencing whole proteins using an imperfect database.AMASS: algorithm for MSI analysis by semi-supervised segmentation.The elusive evidence for chromothripsisTests of selection in pooled case-control data: an empirical study.
P50
Q21089567-1F1934CE-94AE-441E-A349-F468050D9F6EQ21090194-D8DED581-46EC-48D9-8FB7-D77B7513522FQ21145383-4B0F8905-2260-4484-92FC-5C046E8CBB29Q22066287-03783F89-E3BB-47A4-81A5-C6126167AB57Q24564556-81E9BEED-9264-42B7-9BCE-A175AF2CAA5CQ24603900-3898262E-9492-4E36-8A49-DFC573C9DC1CQ24625492-E0DE3614-B3F9-4F26-8588-783B70F65A4DQ24647100-F52AE2DB-BC22-436D-B4F8-54476EEBB92FQ24650630-C3FD82E7-79DC-4696-B9EF-AE40AD40D747Q24676843-9C698527-5EF7-43CA-A98D-B537D15168DCQ27026487-2AB96592-89F3-4CE0-B5EB-C7A9F35C8FE3Q27334735-A14AD475-9451-4C08-A5F5-0F14D06D8D87Q28203188-182A6E0F-2A31-4FA3-BA37-40AE348B81BDQ28548441-75858FA9-E497-4E3E-AB4B-8F4320FCE184Q28732138-17317CCC-3024-4DD0-89F8-5BF6D5676AD8Q28743236-0C18855C-F610-49E4-8D45-DD27CF3BC4DDQ30395320-CF32C3DD-E821-41CA-8EE7-9CEF42D23481Q30647055-E723BD8A-9184-47AD-99F3-C71F051D8A2AQ30651736-F7CE6084-A355-4C05-A529-E0F3391C4638Q30693039-1D3EEF46-77D6-4ED8-B1EC-19CE263E061DQ30831301-9D3C9A79-7732-4144-89B8-4B065DFDCC97Q30855664-AE04DCFB-B395-4FA1-B67C-C380A7B7DED2Q31087752-2E031319-F843-430E-B71C-22BC60951BABQ31168359-63F8DAD0-EC73-4CCB-B6B0-3F9CD1710341Q33239003-82BDAF49-42E1-477B-9C15-FC13384C5420Q33579908-B783B890-712B-4E5D-8C08-C94A12854196Q33611153-5D8B9666-DAB0-4FCA-80B2-676109729683Q33616848-42AEDEB0-82C2-461D-B1EA-2B7E920CD7B3Q33728635-DB4BC020-0098-4A09-8856-9212086B3ECFQ33745003-3E5FBC57-A255-42B2-971D-88362A7C3137Q33745301-0A4ED42B-9A91-4AF0-B4B7-86BD770273FDQ33757745-39A77BBB-512C-4344-9D91-682D74B03E27Q33804091-7CD7BC0F-1D64-4975-8458-751D68C00FEDQ33823403-80FFA0DE-B19B-41E5-9286-B54ABB364692Q33826943-9D150388-6022-456A-B8F8-3D9999DD3CFAQ33877433-BA21C432-D354-43B0-B563-E0D567D87B0AQ33883042-AD79045B-9094-40F3-AE74-99CFDFEDF035Q33975282-E489E582-891D-4900-84FC-D48D5ACD4907Q33983540-C3205BB5-91CB-4FD9-B0CD-27DD3BACA37CQ34149931-FF09C9C8-FEBE-4D84-AEDC-19CFA04231BE
P50
description
Indian bioinformatician
@en
bioinformaticus
@nl
name
Vineet Bafna
@ast
Vineet Bafna
@en
Vineet Bafna
@es
Vineet Bafna
@nl
Vineet Bafna
@sl
বিনীত বাফনা
@bn
type
label
Vineet Bafna
@ast
Vineet Bafna
@en
Vineet Bafna
@es
Vineet Bafna
@nl
Vineet Bafna
@sl
বিনীত বাফনা
@bn
prefLabel
Vineet Bafna
@ast
Vineet Bafna
@en
Vineet Bafna
@es
Vineet Bafna
@nl
Vineet Bafna
@sl
বিনীত বাফনা
@bn
P214
P244
P269
P101
P106
P166
P1960
NzQu5SwAAAAJ
P2038
Vineet_Bafna
P21
P214
P2381
P244
nb2007019149
P2456
b/VineetBafna
P269
P31
P4955
P496
0000-0002-5810-6241
P549
P6634
vineet-bafna-ab2a3810
P691
stk2007405933