Paired-ends sequencing libraries were prepared from L. tarentolae genomic DNA with the Nextera DNA sample prep kit and sequenced on an Illumina HiSeq platform with 101-nucleotides paired-ends reads. Sequence reads were aligned to the L. tarentolae Parrot TarII PacBio genome assembly [22 (link)] using bwa-mem [23 (link)]. Read duplicates were marked using Picard and GATK was applied for single nucleotide variants and small insertions or deletions discovery [24 (link)]. Copy numbers variations were derived from read depth coverage as described earlier [25 (link)].
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