Dear NGS users,
does anyone know if exists a tool/script/program to analyze in PE sequencing reads that are separately mapped in different position/chromosome as singletons (for example because of a traslocation or a long deletions)?
Thanx a lot,
ME
does anyone know if exists a tool/script/program to analyze in PE sequencing reads that are separately mapped in different position/chromosome as singletons (for example because of a traslocation or a long deletions)?
Thanx a lot,
ME