What are the potential reasons for these gaps

Reference no: EM133291160

Recently, the T2T consortium used the latest PacBio and Oxford Nanopore Technologies to sequence and assemble a near-complete human genome of the double haploid pregnancy tumour CHM13.

Question 1: What is the advantage of sequencing and assembling a double haploid genome of a pregnancy tumour rather than the genome of a healthy human individual?
The T2T genome still has some gaps in the sequence.

Question 2: What are the potential reasons for these gaps in the genome sequence and what strategies could be used to fill the gaps?

Reference no: EM133291160

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