Exome libraries and whole-genome libraries were prepared using a modified protocol49 (link). Modifications included: the use of 1,000 ng of treated gDNA, performing only six cycles of PCR amplification and usage of the Agilent SureSelectXT Mouse All Exon Kit for exon target capture. For murine WGS, after adapter ligation, libraries were only amplified by two cycles of PCR. Equimolar quantities of the whole-genome indexed libraries were multiplexed, with 18 libraries per pool. Results from 13 of the 18 libraries were used in our analysis. All pooled libraries were sequenced on an Illumina NovaSeq6000 using the 150-base pair (bp) paired-end format.
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