Results for "Genome Assembly"

Bio-Scripts

  • Tadpole is 250x faster than SPADes assembler !

    ...that mce=1 for low-depth metagenomes. mincountretain=0 (mincr)...may yield more accurate genome size estimation. contigpasses=...reads that cannot be used for assembly. This me...y are very slow for large metagenomes. Overlap parameters (for ov...

    987 days ago

  • Install Packages in Python

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

    973 days ago

  • Installing Covid19 Environment !

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

    935 days ago

  • Bash script to simulate a genome !

    ...ues/33 # Use Drosophila melongaster PacBio assembly cd /genetics/elbers/test/fly2 wget https://ftp.ncbi.nlm.nih.gov/genomes/all/GCA/003/401/745/GCA_0034..._genomic.fna_upper.diploid.fasta.log.txt # genome size bgzip -@75 -cd GCA_003401...

    929 days ago

  • Install mgsc on Ubuntu !

    (abhiENV) [abhi@hn1 output_OM824]$ conda create -n mgsc python=3.6 graphviz numpy Co...active environment, use # # $ conda deactivate mgsc -i [path to your assembly graph] -o [output directory n...

    836 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 fo...} { print >> file; }' < multi.fasta #Another great solution is genome tools (gt), which you can find here: http://genometo...

    835 days ago

  • Install StringTie on ubuntu / Linux !

    #StringTie is a software program to perform transcript assembly and quantification of RNAseq data. The binary distributions are available so to install we can just download this distribution and e...

    835 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 I...

    835 days ago

  • Bash command to explore assembly summary genbank !

    wget https://ftp.ncbi.nlm.nih.gov/genomes/genbank/assembly_summary_genbank.txt pip3 install csvkit csvcut -t -K 1 -c 'excluded_from_refseq' assembly_summary_genbank.txt \ | tail -n +2 | tr ";" "\n" \ | sed -e 's/^ //' -e 's/ $//' | grep -v '""' \ | sort | uniq -c | sort -nr

    780 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...

    647 days ago