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Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination

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The breakpoint region for each patient was determined by aligning Sanger sequencing reads to the HRG obtained from the UCSC Genome Browser using the Sequenchersoftware (Gene Codes Corporation, Ann Arbor, MI, USA). Breakpoint coordinates for each individual have been deposited in National Center for Biotechnology Information database of genomic structural variation (dbVar) and are available under the accession number [dbVar :nstd98].

Monthly Publications Archive

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Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination

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Monthly Publications Archive

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Human endogenous retroviral elements promote genome instability via non-allelic homologous recombination

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