Results for "New Genome"

Bio-Scripts

  • Tadpole is 250x faster than SPADes assembler !

    ...that mce=1 for low-depth metagenomes. mincountretain=0 (mi...may yield more accurate genome size estimation. contigpasse...y are very slow for large metagenomes. Overlap parameters (for...ppears that the merge created new errors, undo it. Java Paramet...

    978 days ago

  • Install Packages in Python

    #Create a conda environment. #Install a Python package in the terminal using conda...a env update -f environment.yml #Adding a Package to your YAML File name: genome-analytics-python channels:...

    963 days ago

  • Installing Covid19 Environment !

    (base) vikas@vikas-Lenovo-ideapad-320-15ISK:~/vinodLab/Genepi$ conda env create -f...structural variants detection) * SILVA 16S rRNA database (needed for reference genome detection in metagenomic data...

    925 days ago

  • Bash script to simulate a genome !

    # Reference https://github.com/chhylp123/hifiasm/issues...elbers/test/fly2 wget https://ftp.ncbi.nlm.nih.gov/genomes/all/GCA/003/401/745/GCA_0034...0174v1_genomic.fna_upper.diploid.fasta.log.txt # genome size bgzip -@75 -cd GCA_0034...

    920 days ago

  • Bash script to split multifasta file !

    #Using awk, we can easily split a file (multi.fa) into chunks of size...;} { print >> file; }' < multi.fasta #Another great solution is genome tools (gt), which you can find here: http://genometools.org/, which has the foll...

    825 days ago

  • Install Varscan on Ubuntu / Linux !

    #Varscan is a java program designed to call variants in sequencing data. It was developed at the Genome Institute at Washington Unive...

    825 days ago

  • Script to rapid genome clustering based on pairwise ANI

    First, create a blast+ database: makeblastdb -in -dbtype nucl -out Next, use megablast from blast+ package to perform all-vs-all blastn of sequences: blastn -query...

    637 days ago

  • Genome Scaffolding and gap filling !

    scaffolding with ARCS v1.0.3 (−c3, −l,4, −a,0.9, −z500, −m50, −20 000, −e30000, −s90). https://github.com/bcgsc/arcs Next, automated gap filling was performed using Sealer v2.0.1 (−L150, -P10, −k75-115 [step = 10]) https://github.com/bcgsc/abyss/tree/sealer-release

    622 days ago

  • Identify genome-wide synteny with LASTZ alignment

    #This is the walkstrough how to identifiy genome-wide synteny markers based on LASTZ alignment. Step1:Mask the repeat sequences for both genomes and chromosomes. RepeatMa...

    519 days ago

  • Perl script to find inverted repeats !

    ...Bio::Tools::Run::RepeatMasker; my $genome_file = "genome.fasta"; # read genome sequence my $seqio = Bio::SeqIO->new(-file => $genome_file, -format =...y $rm = Bio::Tools::Run::RepeatMasker->new(); my $rm_report = $rm->run($genome_file); # parse RepeatMaske...

    427 days ago