Lol..I didn't it is a prank script..
I have another sequence using a whole-genome shotgun strategy of illumina paired-end reads, but this sequence from
another variety belong the same crop. (say for eg. I have WGS sequence of Apple (variety 1 and variety2), If I have
low contig N50 by de novo genome assembling variety 1. Can I combine and variety 1 and variety 2 paired-end reads
and do de novo genome assembly?
I have additional transcriptome sequences from different tissue of variety 1, how can I use this sequence
for genome assembly?
I have another sequence using a whole-genome shotgun strategy of illumina paired-end reads, but this sequence from
another variety belong the same crop. (say for eg. I have WGS sequence of Apple (variety 1 and variety2), If I have
low contig N50 by de novo genome assembling variety 1. Can I combine and variety 1 and variety 2 paired-end reads
and do de novo genome assembly?
I have additional transcriptome sequences from different tissue of variety 1, how can I use this sequence
for genome assembly?
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