- CLoNe: automated clustering based on local density neighborhoods for application to biomolecular structural ensembles
- A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency
- Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach
- Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions
- Cancer immune control dynamics: a clinical data driven model of systemic immunity in patients with metastatic melanoma
- A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency
- Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach
- Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions
- Mechanisms of enhancer action: the known and the unknown
- Publisher Correction: MTSplice predicts effects of genetic variants on tissue-specific splicing
- Improving the completeness of public metadata accompanying omics studies
- Subtype-associated epigenomic landscape and 3D genome structure in bladder cancer
- Publisher Correction: MTSplice predicts effects of genetic variants on tissue-specific splicing
- Improving the completeness of public metadata accompanying omics studies
- ChIP-BIT2: a software tool to detect weak binding events using a Bayesian integration approach
- Survival time prediction by integrating cox proportional hazards network and distribution function network
- Popularity and performance of bioinformatics software: the case of gene set analysis
- Phylogenetic analysis of Harmonin homology domains
- TANTIGEN 2.0: a knowledge base of tumor T cell antigens and epitopes
- Streamlining differential exon and 3′ UTR usage with diffUTR
Whats new in Bioinformatics
Genome Biology
- A verified genomic reference sample for assessing performance of cancer panels detecting small variants of low allele frequency
- Identification of X-chromosomal genes that drive sex differences in embryonic stem cells through a hierarchical CRISPR screening approach
- Cross-oncopanel study reveals high sensitivity and accuracy with overall analytical performance depending on genomic regions
- Mechanisms of enhancer action: the known and the unknown
- Publisher Correction: MTSplice predicts effects of genetic variants on tissue-specific splicing
- Improving the completeness of public metadata accompanying omics studies
- Subtype-associated epigenomic landscape and 3D genome structure in bladder cancer
- PD-L1 lncRNA splice isoform promotes lung adenocarcinoma progression via enhancing c-Myc activity
- Comparative regulomics supports pervasive selection on gene dosage following whole genome duplication
- A benchmark for RNA-seq deconvolution analysis under dynamic testing environments