Hi all,
Does anybody know what is the number of reads (and what coverage per base) which are needed for sequencing of mouse whole genome - in order to detect translocations, using Illumina (HiSeq20000)?
Also - any recommendations on the read length and single/paired end or mate pairs for such purpose?
Thanks.
Does anybody know what is the number of reads (and what coverage per base) which are needed for sequencing of mouse whole genome - in order to detect translocations, using Illumina (HiSeq20000)?
Also - any recommendations on the read length and single/paired end or mate pairs for such purpose?
Thanks.