Results for "DNA Methylation"
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Motif based sequence analysis suits The MEME Suite allows the biologist to discover novel motifs in colle...f other motif-based analyses. The MEME Suite supports motif-based analysis of DNA, RNA an...2704 days ago
- PANDASEQ assembles paired-end Illumina reads into sequences, trying to correct for errors and uncalled bases. Th...robability of the forward and reverse reads having come from a single piece of DNA.3.Ident...
2673 days ago
FSA: Fast Statistical Alignment
FSA is a probabilistic multiple sequence alignment algorithm which uses a "distance-based" approach to aligning homologous protein, RNA or DNA sequenc...2659 days ago
DnaSP v5: a software for comprehensive analysis of DNA polymorphism data
DnaSP is a software package for a comprehensive analysis of DNA polymorphism data. Version 5 implements a number of new features and analytical methods allowing extensive DNA polymor...2659 days ago
- GenomeComp is a tool for summarizing, parsing and visualizing the genome wide sequence comparison results derive...other sequence features like repeat sequence distributions in one whole-genome DNA sequenc...
2648 days ago
DAGchainer: Computing Chains of Syntenic Genes in Complete Genomes
The DAGchainer software computes chains of syntenic genes found within complete genome sequences. As input, DAGc...ing function which accounts for the distance between neighboring genes on each DNA molecul...2648 days ago
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2017
Strand Life Sciences announces the release of Strand NGS v3.1 at ASHG 2...ique Molecular Identifiers (UMIs) for DNA-, RNA-, and small-RNA-Seq. S...e Molecular Identifiers, or UMIs, for DNA-, RNA- and small-RNA-Seq. UMI...ow-grade FFPE samples, UMI support in DNA-Seq ena...2400 days ago
Pacbio Long Reads Compatible Software and Tools
The following software packages are known to be compatible with PacBio® data,...Consensus and variant calling RNA analysis Epigenetic base modifications and methylation Barcoding Genome Browsers...2622 days ago
- DIAMOND is a sequence aligner for protein and translated DNA searches and functions as a drop-in replacement for the NCBI BLAST software tools. It is suitable for protein-protein search as well as DNA-protein...
2579 days ago
- NGS data are just a bunch of sequences, you have no idea which region in the genome each sequences...reference sequence is called mapping. The most used mappers of DNA-seq data are BWA and Bowtie for DNA-Seq dat...
2574 days ago
