validation copy number variations in whole genomes
Hello every one I have a question about the accuracy of copy number variations found in the whole genome how can I validation copy number variations found in the laboratory? which method do you offer for me?
best regards
• 1,668 views
•
link
written
by
askari.arezou94 •
1 answer
Can I use from qPCR to confirming copy number variations?
• 0 views
•
link
written
by
askari.arezou94 •
Log in to answer this question.
More posts like this
-
Find depth of genome
written by askari.arezou94 •
-
can i detect regulatory proteins with co-expression network?
written by askari.arezou94 •
-
Diffrent between design co-Expression network with RNA-Seq data and micoarray data
written by askari.arezou94 •
-
detect structural variants with read depth in whole genome
written by askari.arezou94 •
-
Validation assembly with T.A Cloning
written by askari.arezou94 •
-
how Gap closer can fill gaps in scafolds
written by askari.arezou94 •
-
what the mean of Genomic content
written by askari.arezou94 •
-
mean of k-mer coverage cuttoff
written by askari.arezou94 •
-
Genome draft sequences
written by alzahare1985 •
-
Structural Variants Annotation in SG- ADVISER
written by stefan.mester •
You can easily use FISH or MLPA
Thank you for your response can I use from cloning for confirming validation?
I believe it's possible but never used this approach! Also the qPCR, never used it to validate CNVs.
ook, thank you. actually, I thought coloring and qPCR are the one way to validate CNVs. do you know , why never used from qPCR and Cloning to confirm copy number variations?
We have a pathology lab integrated, so every CNV is confirmed by them using FISH (for somatic). For germline CNVs we use MLPA in the lab.
ook. thank you for response
Excuseme, Can i use from "gfp Crisper" for validation copy number variations?