Author

Rajini Haraksingh

Stanford MedicineORCID 0000-0002-6644-8874Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:variant calling· 2 Assay:whole-genome sequencing· 2 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Alexander Eckehart UrbaniD· 2 shared Bo ZhouiD· 2 shared Reenal PattniiD· 2 shared Steve S. HoiD· 2 shared Xianglong ZhangiD· 2 shared Alexej S. AbyzoviD· 1 shared Dimitri PerriniD· 1 shared Giltae SongiD· 1 shared

Activity by Year

2018-2019 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenomics

Alexander Eckehart UrbanORCID

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2 papers

Recent·Most cited

GenomicsGenome ResearchPeer-reviewedMar 1, 2019

Comprehensive, integrated, and phased whole-genome analysis of the primary ENCODE cell line K562

Bo Zhou, Steve S. Ho, Stephanie Greer…·Alexander Eckehart Urban

The paper provides a comprehensive whole-genome analysis of K562, identifying genomic structural features and their impact on functional genomics data.

123 citations

humanwhole-genome sequencing

𝕏 PostBluesky

GenomicsJournal of Medical GeneticsPeer-reviewedJul 30, 2018

Whole-genome sequencing analysis of copy number variation (CNV) using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis

Bo Zhou, Steve S. Ho, Xianglong Zhang…·Alexander Eckehart Urban

The paper compares low-coverage whole-genome sequencing strategies to array-based methods for detecting copy number variations, finding WGS more efficient and accurate.

95 citationstop 1%

humanwhole-genome sequencing

𝕏 PostBluesky