Depends on your type of library and on the quality of the reads. Give it a try, play around.
Sven
-
Thanks for your reply. It was really helpful.
What about PolyA and PolyT sequences? How long any sub-sequence be to qualify as polyA or polyT.Leave a comment:
-
This all depends heavily on what kind of library (ESTs, gen. shotgun, fosmid pool etc) you are using. This decides if you have any kind of vector and/or adaptors to be removed. If your library is free of any unwanted sequence and you don't see the need for screening before assembly, then fine, go for it.
If not, tools like SSAHA (Sanger Centre), cross_match (WashU), megablast (NCBI) might be of assistance. There are many more.
Some assemblers also provide some kind of clipping functionality (e.g. MIRA).
cheers,
SvenLeave a comment:
-
non paired adapters in 454 data
Can anyone please let me know any preprocessing steps (like cleansing adapters or any other steps) for non paired 454 sequenced data and any available tool that allows the same, before assembling is performed.
Thanks
-
Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.
We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing...
Leave a comment: