Comment on "Tools for Sequence translation !"
...nslation is the process of converting a DNA or RNA sequence into its corresponding protein sequence. This is an important step in the analysis of genomic and transcriptomic data. Ther...435 days ago
Comment on "Tools for RNA classification"
...olecules. RNAmmer: RNAmmer is a tool for predicting rRNA genes in genomic sequences. It uses a combinat...tRNAscan-SE: tRNAscan-SE is a tool for identifying tRNA genes in genomic sequences. It uses a combinat...435 days ago
Comment on "Tools to detect synteny blocks regions among multiple genomes"
...ome synteny analysis is the comparison of the genomic structure and gene content of...the synteny analysis by identifying conserved genomic regions, identifying gene fam...nalysis by comparing them to other sources of genomic data, such as gene expression...437 days ago
Comment on "List of non-commercial NGS genotype-calling software"
...bsp;] manta – Structural variant and indel caller for mapped sequencing data. [ paper-2015 ]gridss – GRIDSS: the Genomic Rearrangement IDentification...1156 days ago
Comment on "Genome in a Bottle (GIAB) Consortium"
...genomes for benchmarking, we have worked with the Global Alliance for Genomics and Health Benchmarking Team...arge indel and structural variant calls, as well as calls in difficult genomic contexts (e.g., homopolymers/...1574 days ago
Comment on "List of genome announcement, notes and reporting journals"
The "Genomic Data" journal also publish genome announcement https://www.journals.elsevier.com/genomics-data/2323 days ago
Comment on "Structural variation: the hidden genomic treasure"
I like this tool GRIDSS: the genomic rearrangement identification software suite. A high-speed next-gen sequencing structural variation caller. GRIDSS calls variants based o...2717 days ago
Comment on "Recombination detection tool"
Using population genomic data http://arxiv.org/ftp/arxiv/papers/1403/1403.4264.pdf to detect recombination hotspot.3028 days ago
Comment on "Tools to detect synteny blocks regions among multiple genomes"
A Fugu–Human Genome Synteny Viewer: web software for graphical display and annotation reports of synteny between Fugu genomic sequence and human genes http://nar.oxfordjournals.org/content/32/8/2618.short3210 days ago
Comment on "Next Generation Sequencing (NGS) Tutorials"
Sequencing depth and coverage: key considerations in genomic analyses https://rtsf.natsci.msu.edu/_rtsf/assets/File/depth%20and%20coverage.pdf3282 days ago