Unconfigured Ad
Collapse
X
-
FYI, BLAT worked well. I created a series of databases, each containing 7.5 million reads.
-
I am currently trying BLAT. Cannot build a database that large so splitting the 300M reads into subsets.Originally posted by GenoMax View PostBlat should work for this too: http://genome.ucsc.edu/FAQ/FAQblat.html#blat3
Leave a comment:
-
-
Using Bioconductor
You can simply do it in R.
1. Install the Biostrings package
source("http://bioconductor.org/biocLite.R")
biocLite("Biostrings")
2. Load the Biostrings package
library(Biostrings)
3. Use the matchPattern function. To get a detailed help page for it, type :
?matchPattern
You'll see it has all of the options that you need for your example.
matchPattern(pattern, subject, max.mismatch=0, min.mismatch=0, with.indels=FALSE, fixed=TRUE, algorithm="auto")
Leave a comment:
-
align short query against 300M Illumina reads
Hi,
I have 8 short (~60nt) query sequences which I want to align to roughly 300M Illumina reads (100bp). Criteria are:
- Allow a few mismatches (< 8)
- Gaps are not allowed.
- Alignment should span the entire query.
- Report all matches, NOT just the best one.
Do any programs exists that can accomplish this task? I was thinking BWA, or other next-gen read mappers, but these usually work with whole genomes as their database and reads as the query. The case I have here is somewhat different and may not work with these programs.
Any ideas?
Thanks in advance for the help.Last edited by hohllp; 11-17-2011, 01:49 PM.Tags: None
Latest Articles
Collapse
-
by SEQadmin2
NGS has revolutionized clinical microbiology by offering new ways to identify and surveil pathogens without prior knowledge of the target. One popular approach is 16S rRNA and ITS amplicon sequencing, which targets specific microbial markers. But studies are increasingly incorporating shotgun metagenomics, a technique that sequences all DNA from a sample without targeting specific microbial markers. This approach allows more detailed taxonomic classification, detection...-
Channel: Articles
Today, 06:46 AM -
-
by SEQadmin2
Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?
Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating...-
Channel: Articles
10-14-2026, 09:55 AM -
ad_right_rmr
Collapse
News
Collapse
| Topics | Statistics | Last Post | ||
|---|---|---|---|---|
|
Genome Sequencing Reveals Large, Repeat-Rich DNA in Trapdoor Spider Named for Stephen Colbert
by SEQadmin2
Started by SEQadmin2, 10-28-2026, 09:57 AM
|
0 responses
22 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:57 AM
|
||
|
Started by SEQadmin2, 10-28-2026, 09:51 AM
|
0 responses
14 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:51 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 11:13 AM
|
0 responses
67 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 11:13 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 10:48 AM
|
0 responses
47 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 10:48 AM
|
Leave a comment: