Monday, 22 September 2014

Papers to Read

Predicting the human epigenome from DNA motifs

SeqControl: process control for DNA sequencing

Accurate de novo and transmitted indel detection in exome-capture data using microassembly

Phen-Gen: combining phenotype and genotype to analyze rare disorders

Detecting and correcting systematic variation in large-scale RNA sequencing data

Normalization of RNA-seq data using factor analysis of control genes or samples

A comprehensive assessment of RNA-seq accuracy, reproducibility and information content by the Sequencing Quality Control Consortium

A community effort to assess and improve drug sensitivity prediction algorithms

A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data

A formal perturbation equation between genotype and phenotype determines the evolutionary action of protein coding variations on fitness

Decoding ChIP-seq with a double-binding signal refines binding peaks to single-nucleotides and predicts cooperative interaction

Genome-wide signals of positive selection in human evolution

Natural variation of histone modification and its impact on gene expression in the rat genome

Global translational reprogramming is a fundamental layer of immune regulation in plants

Architecture of the human interactome defines protein communities and disease networks

Haematopoietic stem and progenitor cells from humanpluripotent stem cells

Chromatin states define tumour-specific T cell dysfunction and reprogramming







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