SRX11247961 X7091 SRP325952 PRJNA703698 The strain X7091 genome was sequenced using a PacBio RS II platform and Illumina HiSeq 4000 platform at the Beijing Genomics Institute(BGI, Shenzhen, China). Four SMRT cells Zero-Mode Waveguide arrays of sequencing, were used by the PacBio platform to generate the subreads set.PacBio subreads (length < 1 kb) were removed. The program Pbdagcon was used for selfcorrection. Draft genomic unitigs, which are uncontested groups of fragments, were assembled using the Celera Assembler against a highquality corrected circular consensus sequence subreads set. To improve the accuracy of the genome sequences, GATK and SOAP tool packages were used to make single-base corrections. SRS9293871 Mycobacterium gordonae subsp. camsnse subsp. nov X7091 X7091 WGS GENOMIC PCR PacBio RS II