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A deconvolution framework that uses single-cell sequencing plus a small benchmark data set for accurate analysis of cell type ratios in complex tissue samples

  • First Published November 25, 2024
Method

Accelerated somatic mutation calling for whole-genome and whole-exome sequencing data from heterogenous tumor samples

  • First Published April 8, 2024
Method

A pedigree-based prediction model identifies carriers of deleterious de novo mutations in families with Li-Fraumeni syndrome

  • First Published August 18, 2020
Method

Combining RT-PCR-seq and RNA-seq to catalog all genic elements encoded in the human genome

  • First Published September 5, 2012
Method

Estimation of alternative splicing variability in human populations

  • First Published November 23, 2011
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