This mostly depends on what you mean by "large amounts" and "large library".
If there are fewer than ~100 short sequences, you could probably get away with enumerating (and indexing) all possible combinations (10,000 total), then doing a simple search.
If you have fewer than ~100,000 short sequences and have predictable start/end points in the library, then you could hash the short sequences and store in memory, then check each ligation product part against the hashed index (unfortunately, using hashes wouldn't allow for errors).
Otherwise, if the library is less than around 1-5GB, you might be better off reversing the query -- create an index of unique ligation products and map the short sequences to those.
Seqanswers Leaderboard Ad
Collapse
Announcement
Collapse
No announcement yet.
X
-
I thought of using -max_target_seqs 2 on command-line blastn providing the two top-hits which will represent which 2 sequences gave rise to the ligation products and then outputting this to a custom BLAST format - I am not sure how to proceed from there to obtain the required tally.
Leave a comment:
-
Tallying BLAST Matches
Hi,
I've got a custom BLASTDB created from a FASTA file containing large amounts of short sequences:
>seqA
GATCGATAGTTAGACTAGTAAGCAAA
>seqB
AAATCACAGTGACTAGTAGAGAGATT
>seqC
AAGGCCCCTATATAGACTGACTAGTA
and so on.
I've sequenced a large library of molecules which are ligation products between 2 of the sequences held in this custom DB i.e. SeqA-SeqC (GATCGATAGTTAGACTAGTAAGCAAAAAGGCCCCTATATAGACTGACTAGTA).
I need to be able to BLAST my sequencing data against the custom database and then tally how many times each possible ligation product is present and output this based on their FASTA labels i.e. something like this:
SeqA-SeqC 54
SeqA-SeqB 102
Is this something that BLAST/BLAST+ may be able to do instrinsically or is it something that would have to be done in perl/python? Does anybody have a script which may do something similar which I could have a look at to get a framework to build upon?
Thanks!
- JuliaTags: None
Latest Articles
Collapse
-
by seqadmin
Innovations in next-generation sequencing technologies and techniques are driving more precise and comprehensive exploration of complex biological systems. Current advancements include improved accessibility for long-read sequencing and significant progress in single-cell and 3D genomics. This article explores some of the most impactful developments in the field over the past year.
Long-Read Sequencing
Long-read sequencing has...-
Channel: Articles
12-02-2024, 01:49 PM -
-
by seqadmin
The field of immunogenetics explores how genetic variations influence immune responses and susceptibility to disease. In a recent SEQanswers webinar, Oscar Rodriguez, Ph.D., Postdoctoral Researcher at the University of Louisville, and Ruben MartÃnez Barricarte, Ph.D., Assistant Professor of Medicine at Vanderbilt University, shared recent advancements in immunogenetics. This article discusses their research on genetic variation in antibody loci, antibody production processes,...-
Channel: Articles
11-06-2024, 07:24 PM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, 12-02-2024, 09:29 AM
|
0 responses
132 views
0 likes
|
Last Post
by seqadmin
12-02-2024, 09:29 AM
|
||
Started by seqadmin, 12-02-2024, 09:06 AM
|
0 responses
48 views
0 likes
|
Last Post
by seqadmin
12-02-2024, 09:06 AM
|
||
Started by seqadmin, 12-02-2024, 08:03 AM
|
0 responses
38 views
0 likes
|
Last Post
by seqadmin
12-02-2024, 08:03 AM
|
||
Started by seqadmin, 11-22-2024, 07:36 AM
|
0 responses
68 views
0 likes
|
Last Post
by seqadmin
11-22-2024, 07:36 AM
|
Leave a comment: