Deal all,
I installed GMAP, and build indexing of draft genome using gmap_build by using this cammand.
/home/yog/software/gmap-2016-11-07/util/gmap_build -D /home/yog/database/ -d custard_genome Custard_1.0.chromosomes.fix.fasta
Now want to align trinity assembled transcript to genome.
my aim is to extract those de novo assembled trinity transcripts that do not able to map on draft genome.
Please suggest how I can do by using GMAP and also share cammand lines.
Thanks Yogesh
Please use a more informative question for your question. In addition, it's good practice to show us what you tried. You should also start with reading the manual.
I am aligning a fastq bacteria reads to my transcriptome assembly using Bowtie2, And shorted the Sam to BAM. The mapped reads file has only one sequence while the bam file has 4.5 Gb data. How it is possible.
Thanks in advance. DEV
I don't see a link between your question and the original question here. Please open a separate thread for your issue and be as informative as possible, including all commands you used.