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Genetics

D-Index
63
Citations
70859
World Ranking
2819
National Ranking
356

Overview

Jennifer Harrow is affiliated with AstraZeneca in the United Kingdom. Their research primarily spans the fields of Biochemistry, Genetics, and Molecular Biology, with a significant focus on Molecular Biology, Information Systems and Management, Genetics, Information Systems, and Cellular and Molecular Neuroscience.

Their work covers a variety of topics, including:

  • Scientific Computing and Data Management
  • Genetics, Bioinformatics, and Biomedical Research
  • Research Data Management Practices
  • RNA and protein synthesis mechanisms
  • Genomics and Phylogenetic Studies
  • Genomics and Rare Diseases
  • Olfactory and Sensory Function Studies

Jennifer Harrow has published in multiple peer-reviewed venues. Frequent publication platforms include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature
  • Bioinformatics
  • Nature Methods
  • Zenodo (CERN European Organization for Nuclear Research)

Notable recent papers authored or coauthored by Jennifer Harrow include:

  • "Introducing the FAIR Principles for research software," 2022, Scientific Data
  • "DOME: recommendations for supervised machine learning validation in biology," 2021, Archivio Istituzionale della Ricerca (Universita Degli Studi Di Milano)
  • "The status of the human gene catalogue," 2023, Nature
  • "Rare variant associations with plasma protein levels in the UK Biobank," 2023, Nature
  • "Expert curation of the human and mouse olfactory receptor gene repertoires identifies conserved coding regions split across two exons," 2020, BMC Genomics

Jennifer Harrow frequently collaborates with other researchers in their field. Regular coauthors include:

  • Fotis Psomopoulos
  • Adam Frankish
  • Salvador Capella-Gutierrez
  • Leyla Jael Castro
  • Paula Andrea Martinez

Best Publications

  • An integrated map of genetic variation from 1,092 human genomes

    Goncalo R Abecasis;Adam Auton;Lisa D Brooks

  • Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project

    Ewan Birney;John A. Stamatoyannopoulos;Anindya Dutta;Roderic Guigó

  • Landscape of transcription in human cells

    Sarah Djebali;Carrie A. Davis;Angelika Merkel;Alex Dobin

  • The GENCODE v7 catalog of human long noncoding RNAs: analysis of their gene structure, evolution, and expression.

    Thomas Derrien;Rory Johnson;Giovanni Bussotti;Andrea Tanzer

  • GENCODE: The reference human genome annotation for The ENCODE Project

    Jennifer Harrow;Adam Frankish;Jose M. Gonzalez;Electra Tapanari

  • The zebrafish reference genome sequence and its relationship to the human genome.

    Kerstin Howe;Matthew D. Clark;Carlos F. Torroja;Carlos F. Torroja;James Torrance

  • An integrated encyclopedia of DNA elements in the human genome

    Ian Dunham;Anshul Kundaje;Shelley F. Aldred;Patrick J. Collins

  • A conditional knockout resource for the genome-wide study of mouse gene function.

    William C. Skarnes;Barry Rosen;Anthony P. West;Manousos Koutsourakis

  • Analyses of pig genomes provide insight into porcine demography and evolution

    Martien A. M. Groenen;Alan L. Archibald;Hirohide Uenishi;Christopher K. Tuggle

  • A User's Guide to the Encyclopedia of DNA Elements (ENCODE)

    Richard M. Myers;John Stamatoyannopoulos;Michael Snyder;Ian Dunham

  • A Systematic Survey of Loss-of-Function Variants in Human Protein-Coding Genes

    Daniel G. MacArthur;Daniel G. MacArthur;Suganthi Balasubramanian;Adam Frankish;Ni Huang

  • The Genome Sequence of Taurine Cattle: A Window to Ruminant Biology and Evolution

    Christine G. Elsik;Christine G. Elsik;Christine G. Elsik;Ross L. Tellam;Kim C. Worley;Kim C. Worley;Richard A. Gibbs

  • Multiple evidence strands suggest that there may be as few as 19 000 human protein-coding genes

    Iakes Ezkurdia;David Juan;Jose Manuel Rodriguez;Adam Frankish

  • Assessment of transcript reconstruction methods for RNA-seq

    Tamara Steijger;Josep F Abril;Pär G. Engström;Pär G. Engström;Felix Kokocinski

  • GENCODE: producing a reference annotation for ENCODE

    Jennifer Harrow;Adam Frankish;Alexandre Reymond;Alexandre Reymond

  • The consensus coding sequence (CCDS) project: Identifying a common protein-coding gene set for the human and mouse genomes

    Kim D. Pruitt;Jennifer Harrow;Rachel A. Harte;Craig Wallin

  • Systematic evaluation of spliced alignment programs for RNA-seq data

    Pär G Engström;Tamara Steijger;Botond Sipos;Gregory R Grant

  • The DNA sequence and biological annotation of human chromosome 1

    S. G. Gregory;S. G. Gregory;K. F. Barlow;K. E. McLay;R. Kaul

  • Variation analysis and gene annotation of eight MHC haplotypes: The MHC Haplotype Project

    Roger Horton;Richard Gibson;Penny Coggill;Marcos Mateo Miretti

  • The GENCODE pseudogene resource

    Baikang Pei;Cristina Sisu;Adam Frankish;Cédric Howald

Frequent Co-Authors

Adam Frankish
Adam Frankish European Bioinformatics Institute
Tim Hubbard
Tim Hubbard King's College London
Roderic Guigó
Roderic Guigó Pompeu Fabra University
Alexandre Reymond
Alexandre Reymond University of Lausanne
Mark Gerstein
Mark Gerstein Yale University
Thomas R. Gingeras
Thomas R. Gingeras Cold Spring Harbor Laboratory
Mark Diekhans
Mark Diekhans University of California, Santa Cruz
Stylianos E. Antonarakis
Stylianos E. Antonarakis University of Geneva
Paul Flicek
Paul Flicek The Jackson Laboratory
Jane Rogers
Jane Rogers Earlham Institute

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