Unconfigured Ad

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts
  • lre1234
    Senior Member
    • Aug 2011
    • 110

    Mate-pair sequence structural variants

    I was given a mate-pair whole genome dataset that was sequenced on a SOLID 5500xl. I was interested in knowing if anyone has had any experience in doing structural variant calling (CNV, LOH, translocations, etc) with using this kind of data, and what the "best" approach. Or if anyone has done structural varaint calling with mate-pair in general and what they used for it.
    Thanks

Latest Articles

Collapse

ad_right_rmr

Collapse

News

Collapse

Topics Statistics Last Post
Started by SEQadmin2, Yesterday, 11:58 AM
0 responses
10 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-05-2026, 10:09 AM
0 responses
25 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-04-2026, 08:59 AM
0 responses
35 views
0 reactions
Last Post SEQadmin2  
Started by SEQadmin2, 06-02-2026, 12:03 PM
0 responses
58 views
0 reactions
Last Post SEQadmin2  
Working...