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Author Details

James K Bonfield
Wellcome Sanger Institute
1994
27
21
PMIDPaper TitleJournal TitlePublished Year
34999766CRAM 3.1: advances in the CRAM file format.Bioinformatics2022
35072136GA4GH: International policies and standards for data sharing across genomic research and healthcare.Cell Genom2021
33594436HTSlib: C library for reading/writing high-throughput sequencing data.Gigascience2021
33590861Twelve years of SAMtools and BCFtools.Gigascience2021
29992288Crumble: reference free lossy compression of sequence quality values.Bioinformatics2019
28638050De novo yeast genome assemblies from MinION, PacBio and MiSeq platforms.Sci Rep2017
27776113Comparison of high-throughput sequencing data compression tools.Nat Methods2016
24930138The Scramble conversion tool.Bioinformatics2014
23533605Compression of FASTQ and SAM format sequencing data.PLoS One2013
19906712Improvements to services at the European Nucleotide Archive.Nucleic Acids Res2010
20513662Gap5--editing the billion fragment sequence assembly.Bioinformatics2010
19909804Genome-wide end-sequenced BAC resources for the NOD/MrkTac() and NOD/ShiLtJ() mouse genomes.Genomics2010
18978013Petabyte-scale innovations at the European Nucleotide Archive.Nucleic Acids Res2009
18039715Priorities for nucleotide trace, sequence and annotation data capture at the Ensembl Trace Archive and the EMBL Nucleotide Sequence Database.Nucleic Acids Res2008
15590942Transcriptome analysis for the chicken based on 19,626 finished cDNA sequences and 485,337 expressed sequence tags.Genome Res2005
16221968Shotgun haplotyping: a novel method for surveying allelic sequence variation.Nucleic Acids Res2005
16257172A genome-wide, end-sequenced 129Sv BAC library resource for targeting vector construction.Genomics2005
15852006Complex haplotypes, copy number polymorphisms and coding variation in two recently divergent mouse strains.Nat Genet2005
11836205ZTR: a new format for DNA sequence trace data.Bioinformatics2002
11836229Trev: a DNA trace editor and viewer.Bioinformatics2002
11449730Sequence assembly and finishing methods.Methods Biochem Anal2001
10547834The Staden package, 1998.Methods Mol Biol2000
9649626Automated detection of point mutations using fluorescent sequence trace subtraction.Nucleic Acids Res1998
8907307Experiment files and their application during large-scale sequencing projects.DNA Seq1996
7753633The application of numerical estimates of base calling accuracy to DNA sequencing projects.Nucleic Acids Res1995
8559656A new DNA sequence assembly program.Nucleic Acids Res1995
79063982.2 Mb of contiguous nucleotide sequence from chromosome III of C. elegans.Nature1994
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Collaborators

European Bioinformatics Institute
Co-authored papers 5
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Co-authored papers 5
The Wellcome Trust Sanger Institute
Co-authored papers 4
European Bioinformatics Institute
Co-authored papers 4
Cancer Research UK Cambridge Institute, University of Cambridge
Co-authored papers 3
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Wellcome Sanger Institute
Co-authored papers 3
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European Bioinformatics Institute
Co-authored papers 3
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BGI Hong Kong Tech Co Ltd.
Co-authored papers 2
The Wellcome Trust Sanger Institute
Co-authored papers 2
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Co-authored papers 2
University of Cambridge
Co-authored papers 2
Johns Hopkins University School of Medicine
Co-authored papers 1
Oregon Health & Science University
Co-authored papers 1
Duke-Margolis Center for Health Policy
Co-authored papers 1
University of Colorado Anschutz Medical Campus
Co-authored papers 1
University of Geneva
Co-authored papers 1
Wellcome Sanger Institute
Co-authored papers 1
Cleveland Clinic
Co-authored papers 1
Ontario Institute for Cancer Research
Co-authored papers 1
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University of Toronto
Co-authored papers 1
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
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Broad Institute of MIT and Harvard
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Genomic Medicine Institute
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Memorial Sloan Kettering Cancer Center
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