Results for "genome announcements"

Bio-Scripts

  • Tadpole is 250x faster than SPADes assembler !

    lege@jit-Lenovo-ideapad-320-15ISK:~/Downloads/MyTools/Vir$ tadpole.sh...mmended that mce=1 for low-depth metagenomes. mincountretain=0 (mincr...may yield more accurate genome size estimation. contigpasse...but they are very slow for large metagenomes. O...

    975 days ago

  • Install Packages in Python

    #Create a conda environment. #Install a Python package in the terminal using conda. $ conda create -n myenv...nv update -f environment.yml #Adding a Package to your YAML File name: genome-analyt...

    961 days ago

  • Installing Covid19 Environment !

    (base) vikas@vikas-Lenovo-ideapad-320-15ISK:~/vinodLab/Genepi$ conda env create -f covid19-environment.yml Colle...uctural variants detection) * SILVA 16S rRNA database (needed for reference genome detect...

    923 days ago

  • Bash script to simulate a genome !

    # Reference https://github.com/chhylp123/hifiasm/issues/33 # Use Drosophila melonga...bers/test/fly2 wget https://ftp.ncbi.nlm.nih.gov/genomes/all/GCA/003/401/745/GCA_0034...74v1_genomic.fna_upper.diploid.fasta.log.txt # genome size...

    917 days ago

  • Bash script to split multifasta file !

    #Using awk, we can easily split a file (multi.fa) into chunks of size N (here, N=500), by using the f...{ print >> file; }' < multi.fasta #Another great solution is genome tools (gt), which you can find here: http://genometools.o...

    822 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 Instit...

    822 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 -...

    634 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

    619 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 c...

    516 days ago

  • Perl script to find inverted repeats !

    #!/usr/bin/perl use strict; use warnings; use Bio::SeqIO; use Bio::Tools::Run::RepeatMasker; my $genome_file = "genome.fasta"; # read genome sequ...RepeatMasker->new(); my $rm_report = $rm->run($genome_file);...

    424 days ago