Insaflu

DeepVariant — CNN-based variant caller that converts aligned reads into pileup image tensors and classifies them with a deep neural network to produce SNP and indel calls in VCF/gVCF format. Supports

1 shared topic • 2 shared operations

GRIDSS (Genomic Rearrangement IDentification Software Suite) is a modular structural variant and breakend caller for Illumina short-read data that combines alignment-guided positional de Bruijn graph

1 shared topic • 2 shared operations

MIDORI Reference 2 (MIDORI2) is a curated reference database of eukaryotic mitochondrial DNA and amino acid sequences used for taxonomic assignment of environmental and metabarcoding samples. It provi

1 shared topic • 2 shared operations

vConTACT2 (Viral Contig Automatic Cluster Taxonomy 2) clusters prokaryotic viral genomes and contigs by shared protein content to assign taxonomy context from reference viral genomes. Use when working

1 shared topic • 2 shared operations

PubMed Database — NCBI's comprehensive biomedical literature database providing free access to over 37 million citations from MEDLINE, life science journals, and online books. Query via E-utilities RE

1 shared topic • 1 shared operation