Fastq2vcf: a concise and transparent pipeline for whole-exome sequencing data analyses

Overview of attention for article published in BMC Research Notes, March 2015

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So far, Dimensions has found 15 publications that cite this research output.

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Resources and tools for rare disease variant interpretation

Article in Frontiers in Molecular Biosciences (May 2023)

JWES: a new pipeline for whole genome/exome sequence data processing, management, and gene‐variant discovery, annotation, prediction, and genotyping

Article in FEBS Open Bio (August 2021)

Genomics pipelines to investigate susceptibility in whole genome and exome sequenced data for variant discovery, annotation, prediction and genotyping

Article in PeerJ (July 2021)

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