<![CDATA[BOL: Related items]]> https://bioinformaticsonline.com/related/26852?offset=1370 https://bioinformaticsonline.com/blog/view/38765/list-of-tools-frequently-used-while-genome-assembly Tue, 22 Jan 2019 09:39:02 -0600 https://bioinformaticsonline.com/blog/view/38765/list-of-tools-frequently-used-while-genome-assembly <![CDATA[List of tools frequently used while genome assembly]]> List of tools frequently used while genome assembly:

I have used the following assemblers

I have used the following mappers

I have used the following polishing tools

I have used the following tools to assess genome assembly characteristics

If you have any ideas or superior tools we have missed please let us know in the comments.

]]> BioStar https://bioinformaticsonline.com/bookmarks/view/41996/wgd%E2%80%94simple-command-line-tools-for-the-analysis-of-ancient-whole-genome-duplications Thu, 23 Jul 2020 05:49:45 -0500 https://bioinformaticsonline.com/bookmarks/view/41996/wgd%E2%80%94simple-command-line-tools-for-the-analysis-of-ancient-whole-genome-duplications <![CDATA[wgd—simple command line tools for the analysis of ancient whole-genome duplications]]> wgd is a easy to use command-line tool for KS distribution construction named wgd. The wgd suite provides commonly used KS and colinearity analysis workflows together with tools for modeling and visualization, rendering these analyses accessible to genomics researchers in a convenient manner.

https://academic.oup.com/bioinformatics/article/35/12/2153/5162749

Address of the bookmark: https://github.com/arzwa/wgd

]]> LEGE https://bioinformaticsonline.com/blog/view/43260/bioinformatics-tools-for-telomere-to-telomere-assembly Tue, 17 Aug 2021 13:17:09 -0500 https://bioinformaticsonline.com/blog/view/43260/bioinformatics-tools-for-telomere-to-telomere-assembly <![CDATA[Bioinformatics tools for telomere to telomere assembly !]]> ● Merfin – k-mer-based assembly and variant calling evaluation for improved consensus accuracy (Arang Rhie)
● PanGenie – algorithm that leverages a pangenome reference built from haplotype-resolved genome assemblies in conjunction with k-mer count information from raw, short-read sequencing data to genotype a wide spectrum of genetic variation (Tobias Marschall)
● SQANTI3 – an automated pipeline for the classification of long-read transcripts that can assess the quality of data and the preprocessing pipeline (Rocío Amorín de Hegedüs @rocioadh)
● tama (Transcriptome Annotation by Modular Algorithms) – software designed for processing Iso-Seq data and other long-read transcriptome data (Richard Kuo @GenomeRIK)
● pbaa (PacBio Amplicon Analysis) – separates complex mixtures of amplicon targets from genomic samples to cluster and generate high-quality consensus sequences from HiFi reads (Zev Kronenberg @zevkronenberg)
● bellerophon – analyzes MHC typing and other low-complexity gene amplicon data; performs allele calling while detecting polymorphic sites within the sequences and removing potential chimeric sequence variants (Yuanyuan Cheng @Yuanyuan929)
● svpack – tools for filtering, comparing, and annotating structural variant (SV) calls in VCF format (Aaron Wenger)
● JumboDB – tool for de Bruijn graph construction (Anton Bankevich @AntonBankevich)
● uLTRA – tool for splice alignment of long transcriptomic reads to a genome, guided by a database of exon annotations. (Kristoffer Sahlin @krsahlin)
● LeafGo – workflow to rapidly produce high-quality de novo plant genomes (Luca Ermini @ermini_luca)

Reference:

https://www.pacb.com/blog/young-investigators-share-stellar-science-career-advice-and-bioinformatics-tools-at-smrt-leiden-2021/

 

]]> BioStar https://bioinformaticsonline.com/bookmarks/view/43791/comparative-genomics-visualisation-tools Thu, 17 Feb 2022 05:37:55 -0600 https://bioinformaticsonline.com/bookmarks/view/43791/comparative-genomics-visualisation-tools <![CDATA[Comparative genomics visualisation tools !]]> Comparative genomics visualisation tools !

Address of the bookmark: https://cmdcolin.github.io/awesome-genome-visualization/?latest=true&selected=%23BRIG&tag=Comparative

]]> Neel https://bioinformaticsonline.com/pages/view/44672/libraries-or-management-tools-for-high-throughput-sequencing-data Fri, 04 Oct 2024 02:45:06 -0500 https://bioinformaticsonline.com/pages/view/44672/libraries-or-management-tools-for-high-throughput-sequencing-data <![CDATA[Libraries or management tools for high throughput sequencing data]]>
  • GATB Library. The Genome Analysis Toolbox with de-Bruijn graph. A large part of tools developed by the GenScale team are based on this library.
    These methods enable the analysis of data sets of any size on multi-core desktop computers, including very huge amount of reads data coming from any kind of organisms such as bacteria, plants, animals and even complex samples (e.g. metagenomes). Among them are (the full is available here: https://gatb.inria.fr/software/):
  • LRez: C++ Library and toolkit for the barcode-based management and indexation of linked-read datasets.

    • Variant calling and/or genotyping

    • DiscoSNP++ and discoSnpRAD: Reference-free small variant discovery (SNPs and indels)
    • MindTheGap: Detection and assembly of large insertion variants
    • TakeABreak: reference-free inversion discovery tool
    • SVJedi: Structural Variant genotyper with long read data
    • SVJedi-graph: Structural Variant genotyper with long read data using a variation graph

    Sequence assembly

    • MinYS: reference-guided genome assembly in metagenomics data
    • MTG-link: local assembly tool for linked-read data
    • Minia: De novo short read assembler
    • de-novo pipeline: de-novo assembly pipeline (error correction / contigs / scaffolding) for genomes and meta-genomes
    • Mapsembler2: Targeted assembly (not maintained)

    Managing k-mers & indexation

    • findere: simple strategy for speeding up queries and for reducing false positive calls from any Approximate Membership Query data structure.
      • fimpera extends findere adding the abundance information.
    • kmtricks: modular tool suite for counting kmers, and constructing Bloom filters or kmer matrices, for large collections of sequencing data.
    • kmindex is a tool for indexing and querying sequencing samples. It is built on top of kmtricks.
    • back to sequences: Find sequences (reads, unitigs, genes) related to a set of kmers in large datasets, in a matter of seconds.
    • Backpack Quotient Filter: k-mer indexing data structure with abundance
    • short read connector: Detect similar reads from potentially large read set
    • DSK: Count K-mer in sequences

    Pangenome graph manipulation

    • Pancat: Pangenome Comparison and Analysis Toolkit
    • GFAGraphs: a Python library to handle pangenome graph files in GFA format.

    Comparative metagenomics with k-mers

    Species and bacterial strains identification

    • ORI: software using long nanopore reads to identify bacteria present in a sample at the strain level
    • StrainFLAIR: STRAIN-level proFiLing using vArIation gRaph

    General-purpose sequencing data manipulation

    • GASSST: long read mapper
    • Leon: short read compressor (now included in GATB-core)
    • Bloocoo: short read corrector
    • BCALM: Construct compacted de Bruijn graphs (unitigs)

     Protein Structure

    • A_Purva: Contact Map Overlap solver
    • MD-Jeep: Distance Geometry solver
    • CSA: Comparative Structural Alignment

    Workflow

    • SLICEE: parallel execution of bioinformatics workflows

    Comparative Genomics

    • CASSIS: detection of rearrangement breakpoints
    • PLAST: intensive bank-to-bank sequence comparison
    • DRJBreakpointFinder: detection and precise localization of excision sites in proviral segments
    ]]>     LEGE     https://bioinformaticsonline.com/opportunity/view/17505/kau-thrissur-biotechbioinformatics-rasrfjrftraineestudentships Fri, 26 Sep 2014 20:07:28 -0500 <![CDATA[KAU Thrissur Biotech/Bioinformatics RA/SRF/JRF/Trainee/Studentships]]> Applications are invited from eligible candidates for the following posts at Bioinformatics Centre (DIC), IT- BT Complex, College of Horticulture, Kerala Agricultural University, Vellanikkara, Thrissur.

    1. Research Associate
    Emoluments*: 14880/- + HRA
    Qualification needed: Ph.D/M.Sc in Bioinformatics or Ph.D/M.Sc in Agriculture or Biotechnology with advanced Diploma in Bioinformatics
    Desirable: 2 year experience in Bioinformatics.

    2 Senior Research Fellow
    Emoluments*: 10230/-
    Qualification needed: M.Sc/ M.tech in Bioinformatics or M.Sc in Agriculture/ Biotechnology with Diploma in Bioinformatics.
    Desirable: One year experience in Bioinformatics

    3 Junior Research Fellow
    Emoluments*: 9300/-
    Qualification needed: M.Sc/ M.tech in Bioinformatics or M.Sc in Agriculture/Biotechnology/Plant Sciences with Diploma in Bioinformatics.

    4 .Trainee/Studentship Bioinformatics
    Emoluments*: 5000/-
    Qualification needed: M.Sc in Bioinformatics with good knowledge of Bioinformatics softwares and tools.

    5 Trainee/ Studentship Biotechnology
    Emoluments*: 5000/-
    Qualification needed: M.Sc in Biotechnology, with working knowledge in tissue culture, molecular markers and cloning of genes.

    Candidates with the required qualifications and experience may give an application in the prescribed format with attested copies of certificates to prove eligibility on or before 30th November 2014. The applications are to be addressed to The Associate Dean, College of Horticulture and send to "Professor & Coordinator, Bioinformatics Centre (DIC), IT-BT Complex, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala 680 656”. The envelope may be superscribed “Application for the post at Bioinformatics Centre”.

    *Emoluments are likely to be revised in 2014-2015

    More at http://www.kaubic.in/downloads/Notification_bic.pdf
    http://www.kaubic.in/downloads/Application%20form.pdf

    ]]>