Hi, I have pair end illumina RNA seq data, each sample was ran on 2 lanes. What is the best way to process data of this kind? Do I just combine the rawdata or I process them separately?
Unconfigured Ad
Collapse
X
-
Depends on your computation environment more than anything I'd say. Sometimes its nice to run the alignment in parallel at the same time, one lane at a time, or certain steps are to memory intensive for you enviroment if you put them all together. Sometimes worth testing both to see what works best for you. For instance if you use BWA to align and Samtools I'm not sure which is faster;
cat lanes together
bwa aln, sam generation
samtools sam-->bam, sort, index
or
run lanes separate (2 at a time if you can) with
bwa aln, sam generation
samtools sam-->bam, sort, merge, index
so in that example it is a question of if you can run in parallel or not?, do you have enough resources to sort all the lanes together, is samtools merge of parallel runs faster than aln all at once.
My guess is that running in parallel is much faster if you have the resources to do this, which most standard boxes purchased in the last year (dual hexa-core systems with at least 16Gb ram) should be able to do at least 2 lanes at a time easily
Comment
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
Yesterday, 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
25 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:57 AM
|
||
|
Started by SEQadmin2, 10-28-2026, 09:51 AM
|
0 responses
15 views
0 reactions
|
Last Post
by SEQadmin2
10-28-2026, 09:51 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 11:13 AM
|
0 responses
71 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 11:13 AM
|
||
|
Started by SEQadmin2, 10-22-2026, 10:48 AM
|
0 responses
48 views
0 reactions
|
Last Post
by SEQadmin2
10-22-2026, 10:48 AM
|
Comment