Hi,
I am new to NGS analysis and we have a project for identifying genomic rearrangements. I have gone through several papers and in the recent time there has been a rise in the number of different softwares and algorithms. and now I'm confused, how do I choose which one is better. Apart from the insertion, deletion, inversions and translocations I also need to find amplifications (copy number variation). I was thinking of a combination of softwares for the study. What is everyones opinion. Please give me some guidance.
Thanks.
Shruti
I am new to NGS analysis and we have a project for identifying genomic rearrangements. I have gone through several papers and in the recent time there has been a rise in the number of different softwares and algorithms. and now I'm confused, how do I choose which one is better. Apart from the insertion, deletion, inversions and translocations I also need to find amplifications (copy number variation). I was thinking of a combination of softwares for the study. What is everyones opinion. Please give me some guidance.
Thanks.
Shruti
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