Commandline for paired end reads simulation with BBMap !
(JitMetaENV) ➜ mixedSample git:(main) ✗ /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=1...1004 days ago
Tadpole is 250x faster than SPADes assembler !
lege@jit-Lenovo-ideapad-320-15ISK:~/Downloads/MyTools/Vir$ tadpol...correction or extension. reads=-1 Only process th...r the primary kmer counts. threads=X Spawn X hashing t...(minc) Do not write contigs shorter than this. mincoverage=1...ck=t Undo changes to reads t...990 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 ${b...968 days ago
942 days ago
Bash script to simulate a genome !
# Reference https://github.com/chhylp123/hifiasm/issues/33 # Use Drosophila melon...pe0.fasta.gz # make reference for randomreads.sh # randomreads.sh part of BBTools/BBMap http...max 12000bp /genetics/elbers/bbmap-38.86/randomreads.s...931 days ago
881 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.sam832 days ago
Bash command to count reads in fastq file !
#ref fastq file #ref1_1.fq) echo $(( $(wc -l805 days ago
Awk command to keep only short the fasta header !
awk '/^>/ {$0=$1} 1' file.fasta723 days ago
606 days ago