hello!
I have a problem about GS FLX+(the latest instrument).
1. we recovery the capture beads which have enriched DNA a few days ago, melt solation(NaOH) went into microcentrifuge tube (with capture beads, enriched DNA) on MPC, then there are any capture beads in supernatant?
2. I use GS De novo assembler to Splice a set of MiSeq datas(1X150), it was aborted when several hour, and some errors appear in the display. can i use GS De novo assembler to analyse illumina datas?
Thank you ahead of time,
liuchunlei
I have a problem about GS FLX+(the latest instrument).
1. we recovery the capture beads which have enriched DNA a few days ago, melt solation(NaOH) went into microcentrifuge tube (with capture beads, enriched DNA) on MPC, then there are any capture beads in supernatant?
2. I use GS De novo assembler to Splice a set of MiSeq datas(1X150), it was aborted when several hour, and some errors appear in the display. can i use GS De novo assembler to analyse illumina datas?
Thank you ahead of time,
liuchunlei
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