- A phylogenetic C interpreter for TNT
- QuartataWeb: integrated chemical-protein-pathway mapping for polypharmacology and chemogenomics
- Gcluster: a simple-to-use tool for visualizing and comparing genome contexts for numerous genomes
- PolishEM: image enhancement in FIB-SEM
- Dual-Dropout Graph Convolutional Network for Predicting Synthetic Lethality in Human Cancers
- A random forest based computational model for predicting novel lncRNA-disease associations
- Exploiting sequence labeling framework to extract document-level relations from biomedical texts
- HeMoQuest: a webserver for qualitative prediction of transient heme binding to protein motifs
- debCAM: a Bioconductor R package for fully unsupervised deconvolution of complex tissues
- CNV-BAC: Copy Number Variation Detection in Bacterial Circular Genome
- Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
- DeepMILO: a deep learning approach to predict the impact of non-coding sequence variants on 3D chromatin structure
- Diverse genetic mechanisms underlie worldwide convergent rice feralization
- Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
- DeepMILO: a deep learning approach to predict the impact of non-coding sequence variants on 3D chromatin structure
- Diverse genetic mechanisms underlie worldwide convergent rice feralization
- CRiSP: Accurate Structure Prediction of Disulfide-Rich Peptides with Cystine-Specific Sequence Alignment and Machine Learning
- A Cas12a ortholog with stringent PAM recognition followed by low off-target editing rates for genome editing
- A Cas12a ortholog with stringent PAM recognition followed by low off-target editing rates for genome editing
- High-resolution Repli-Seq defines the temporal choreography of initiation, elongation and termination of replication in mammalian cells
Whats new in Bioinformatics
Genome Biology
- Characterisation of genetic regulatory effects for osteoporosis risk variants in human osteoclasts
- DeepMILO: a deep learning approach to predict the impact of non-coding sequence variants on 3D chromatin structure
- Diverse genetic mechanisms underlie worldwide convergent rice feralization
- A Cas12a ortholog with stringent PAM recognition followed by low off-target editing rates for genome editing
- High-resolution Repli-Seq defines the temporal choreography of initiation, elongation and termination of replication in mammalian cells
- Tandem CTCF sites function as insulators to balance spatial chromatin contacts and topological enhancer-promoter selection
- Obstacles to detecting isoforms using full-length scRNA-seq data
- HiNT: a computational method for detecting copy number variations and translocations from Hi-C data
- Decode-seq: a practical approach to improve differential gene expression analysis
- VALOR2: characterization of large-scale structural variants using linked-reads