This repository contains:1. Starting peptide data, R scripts to process them, and the resulting quantitative protein data2. R scripts to process the genetic data for the Collaborative Cross and Divers
Spinal muscular atrophy (SMA) is a leading genetic cause of infant death, characterised primarily by a loss of lower motor neurons. SMA is caused by mutations in the survival motor neuron 1 (SMN1) gen
We identified 24,431 protein isoforms encoded by 19,914 genes across 34 normal tissues using high-resolution mass spectrometry. This includes 7,693 protein isoforms corresponding to 5,875 genes which
