1066 days ago
1008 days ago
Commandline for paired end reads simulation with BBMap !
.../home/urbe/Tools/bbmap/randomreads.sh ref=mixed.fa out=reads_BBMAP250.fq paired interleave...s/bbmap/current/ align2.RandomReads3 build=1 ref=mixed.fa out=rea...3 [build=1, ref=mixed.fa, out=reads_BBMAP250.fq, paired, interlea...paired=true read length=250 reads=100000 insert size=400-600...1002 days ago
Tadpole is 250x faster than SPADes assembler !
...r the primary kmer counts. threads=X Spawn X hashing t...xtend: Extend sequences to be longer, and optionally...ck=t Undo changes to reads that have lower coverage for...) Discard shavings up to this long. Note: Shave and rinse can pr...988 days ago
Trim the reads in loop using Trimmomatic !
for infile in *_1.fastq.gz do base=$(basename ${infile} _1.fastq.gz) trimmomatic PE ${infile} ${base}_2.fastq.gz \ ${base}_1.trim.fastq.gz ${...967 days ago
940 days ago
Bash script to simulate a genome !
...issues/33 # Use Drosophila melongaster PacBio assembly cd /gen...# make reference for randomreads.sh # randomreads.sh part of BBTools/BBMap http...dea of k-mer with that produces longest N50 # http://kmergenie.bx....netics/elbers/bbmap-38.86/randomreads.sh build=1 \ ow=t seed=1 \...929 days ago
BBmap the reads with all alignments !
bbmap.sh in=../reference/reference.numbered.fa ambig=all vslow perfectmode maxsites=100000 out=fetch_Ids_for_barcode.sam830 days ago
Bash command to count reads in fastq file !
#ref fastq file #ref1_1.fq) echo $(( $(wc -l803 days ago
Extract the mapped and unmapped reads !
PROCESSORS=20 #Single_End_Layout: samtools view --threads $PROCESSORS -b -F 4 in.bam > mapped.bam samtools view --threads $PROCESSORS -b -f 4 in.bam >...m #Paired_End_Layout samtools view --threads $PROCESSORS -b -f 2 in.bam >...602 days ago