Searching journal content for Aravinda Chakravarti in author.

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  1. In memoriam: C. Thomas Caskey (1938–2022)
    • Richard A. Gibbs,
    • Aravinda Chakravarti,
    • Evan E. Eichler,
    • Eric D. Green,
    • Richard M. Myers,
    • Anne C. Ferguson-Smith,
    • Kateryna D. Makova,
    • and Hillary E. Sussman
    Genome Res. March 2022 32: vii-viii; Published in Advance February 17, 2022, doi:10.1101/gr.276658.122
    OPEN ACCESS ARTICLE
  2. In memoriam: Deborah A. Nickerson (1954 –2021)
    • Aravinda Chakravarti,
    • Evan E. Eichler,
    • Richard A. Gibbs,
    • Eric D. Green,
    • Richard M. Myers,
    • and Hillary E. Sussman
    Genome Res. February 2022 32: v-vi; Published in Advance January 24, 2022, doi:10.1101/gr.276582.122
    OPEN ACCESS ARTICLE
  3. Research: A multi-enhancer RET regulatory code is disrupted in Hirschsprung disease
    • Sumantra Chatterjee,
    • Kameko M. Karasaki,
    • Lauren E. Fries,
    • Ashish Kapoor,
    • and Aravinda Chakravarti
    Genome Res. December 2021 31: 2199-2208; Published in Advance November 15, 2021, doi:10.1101/gr.275667.121
  4. Method: Sequence-based correction of barcode bias in massively parallel reporter assays
    • Dongwon Lee,
    • Ashish Kapoor,
    • Changhee Lee,
    • Michael Mudgett,
    • Michael A. Beer,
    • and Aravinda Chakravarti
    Genome Res. September 2021 31: 1638-1645; Published in Advance July 20, 2021, doi:10.1101/gr.268599.120
  5. Method: Human cardiac cis-regulatory elements, their cognate transcription factors, and regulatory DNA sequence variants
    • Dongwon Lee,
    • Ashish Kapoor,
    • Alexias Safi,
    • Lingyun Song,
    • Marc K. Halushka,
    • Gregory E. Crawford,
    • and Aravinda Chakravarti
    Genome Res. October 2018 28: 1577-1588; Published in Advance August 23, 2018, doi:10.1101/gr.234633.118
    OPEN ACCESS ARTICLE
  6. Insight/Outlook: Genomic contributions to Mendelian disease
    • Aravinda Chakravarti
    Genome Res. May 2011 21: 643-644; doi:10.1101/gr.123554.111
  7. LETTER: Human embryonic stem cells have a unique epigenetic signature
    • Marina Bibikova,
    • Eugene Chudin,
    • Bonnie Wu,
    • Lixin Zhou,
    • Eliza Wickham Garcia,
    • Ying Liu,
    • Soojung Shin,
    • Todd W. Plaia,
    • Jonathan M. Auerbach,
    • Dan E. Arking,
    • Rodolfo Gonzalez,
    • Jeremy Crook,
    • Bruce Davidson,
    • Thomas C. Schulz,
    • Allan Robins,
    • Aparna Khanna,
    • Peter Sartipy,
    • Johan Hyllner,
    • Padmavathy Vanguri,
    • Smita Savant-Bhonsale,
    • Alan K. Smith,
    • Aravinda Chakravarti,
    • Anirban Maitra,
    • Mahendra Rao,
    • David L. Barker,
    • Jeanne F. Loring,
    • and Jian-Bing Fan
    Genome Res. September 2006 16: 1075-1083; Published in Advance August 9, 2006, doi:10.1101/gr.5319906
    OPEN ACCESS ARTICLE
  8. Methods: On the probability that a novel variant is a disease-causing mutation
    • Adele A. Mitchell,
    • Aravinda Chakravarti,
    • and David J. Cutler
    Genome Res. July 2005 15: 960-966; Published in Advance June 17, 2005, doi:10.1101/gr.3761405
  9. Methods: Haplotype and Missing Data Inference in Nuclear Families
    • Shin Lin,
    • Aravinda Chakravarti,
    • and David J. Cutler
    Genome Res. August 2004 14: 1624-1632; Published in Advance July 15, 2004, doi:10.1101/gr.2204604
  10. LETTER: The Human MitoChip: A High-Throughput Sequencing Microarray for Mitochondrial Mutation Detection
    • Anirban Maitra,
    • Yoram Cohen,
    • Susannah E.D. Gillespie,
    • Elizabeth Mambo,
    • Noriyoshi Fukushima,
    • Mohammad O. Hoque,
    • Nila Shah,
    • Michael Goggins,
    • Joseph Califano,
    • David Sidransky,
    • and Aravinda Chakravarti
    Genome Res. May 2004 14: 812-819; doi:10.1101/gr.2228504
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