The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data

Overview of attention for article published in Nucleic Acids Research, October 2014

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In the top 25% of all research outputs scored by Altmetric
High Attention Score compared to outputs of the same age (93rd percentile)
High Attention Score compared to outputs of the same age and source (91st percentile)

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blogs: 2 blogs
twitter: 22 X users

googleplus: 1 Google+ user

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https://t.co/NMcDrIfd92 NAR https://t.co/ov8rceuRuA posted by friends: (1) kshameer: Great to note that.... Strongly believe RNAseq i…

RT @kshameer: Great to note that.... Strongly believe RNAseq is a sustainable way to scale genomics. Eg. https://t.co/oZuq2zkT1D https://…

Great to note that.... Strongly believe RNAseq is a sustainable way to scale genomics. Eg. https://t.co/oZuq2zkT1D https://t.co/80c10n4vNO

@chrisamiller @SCEdmunds @michaelhoffman Or call expressed genetic variants using pipelines like eSNV-Detect? https://t.co/AwEvwxiACU

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