Results for "Sequence"

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  • I-PV: Interactive Protein Sequence Visualization

    I-PV is a interactive data visualization software designed for inspection of protein sequences and mutation information. It is mainly used for Genetics and Bioinformatics. So what exactly makes it standout? http://i-pv.org/ipv_rec

    Tags: I-PV, Interactive, Protein, Sequence, Visualization

    2488 days ago

  • Sequence - Evolution - Function; Computational Approaches in Comparative Genomics

    Sequence - Evolution - Function is an introduction to the computational approaches that play a critical role in the emerging new branch of biology known as functional genomics. The book provides the reader with an understanding of the principles and approaches of functional genomics and of t...

    Tags: Sequence, Evolution, Function, Computational, Approaches, Comparative, Genomics

    2454 days ago

  • FOGSAA: Fast Optimal Global Sequence Alignment Algorithm

    Sequence alignment algorithms are widely used to infer similarirty and the point of differences between pair of sequences. FOGSAA is a fast Global alignment algorithm. It is basically a branch and bound approach which starts branch expansion in a greedy way taking the symbols from the given pair ...

    Tags: FOGSAA, Fast, Optimal, Global, Sequence, Alignment, Algorithm

    2330 days ago

  • Get the sequences using coordinates in bed file. $ bedtools getfasta -fi input_file.fa -bed regions_file.bed #Bed #Extract #Sequence #bedtools

    Tags: Bed, Extract, Sequence, bedtools

    2234 days ago

  • GAPPadder: A Sensitive Approach for Closing Gaps on Draft Genomes with Short Sequence Reads

    This software is provided ``as is” without warranty of any kind. In no event shall the author be held responsible for any damage resulting from the use of this software. The program package, including source codes, executables, and this documentation, is distributed free of charge. If you u...

    Tags: GAPPadder, Sensitive, Approach, Closing, Gaps, Draft, Genomes, Short, Sequence, Reads, Genome, Assembly

    2173 days ago

  • BEAP: Blast Extension and Assembly Program

    The Blast Extension and Assembly Program (BEAP) is a computer program that uses a short starting DNA fragment, often a EST or partial gene segment, as "primer", to recursively blast nucleotide databases in an attempt to obtain all sequences that overlaps, directly or indirectly, with the "primer"...

    Tags: BEAP, Blast, Extension, Assembly, Program, Extend, Contigs, Sequence

    2145 days ago

  • ASAR: Advanced metagenomic Sequence Analysis in R

    An interactive data analysis tool for selection, aggregation and visualization of metagenomic data is presented. Functional analysis with a SEED hierarchy and pathway diagram based on KEGG orthology based upon MG-RAST annotation results is available. To read the manual, please click the link&nbs...

    Tags: ASAR, Advanced, metagenomic, Sequence, Analysis, R, NGS, Genomics, Genome

    2117 days ago

  • Platypus: A Haplotype-Based Variant Caller For Next Generation Sequence Data

    Platypus is a tool designed for efficient and accurate variant-detection in high-throughput sequencing data. By using local realignment of reads and local assembly it achieves both high sensitivity and high specificity. Platypus can detect SNPs, MNPs, short indels, replacements and (using th...

    Tags: Platypus, Haplotype-Based, Variant, Caller, Next, Generation, Sequence, Data, NGS, SNP

    2009 days ago

  • The aim of this program suite is to support checks of #Sequence #Variant #Nomenclature according to the guidelines of the #Human #Genome #Variation Society. https://www.mutalyzer.nl/

    Tags: Sequence, Variant, Nomenclature, Human, Genome, Variation

    1910 days ago

  • Alignment-free sequence comparison: benefits, applications, and tools https://genomebiology.biomedcentral.com/articles/10.1186/s13059-017-1319-7 #Alignment #Sequence

    Tags: Alignment, Sequence

    1708 days ago