Header Leaderboard Ad
Collapse
Try to further accelerate Bowtie2 alignment
Collapse
Announcement
Collapse
SEQanswers June Challenge Has Begun!
The competition has begun! We're giving away a $50 Amazon gift card to the member who answers the most questions on our site during the month. We want to encourage our community members to share their knowledge and help each other out by answering questions related to sequencing technologies, genomics, and bioinformatics. The competition is open to all members of the site, and the winner will be announced at the beginning of July. Best of luck!
For a list of the official rules, visit (https://www.seqanswers.com/forum/sit...wledge-and-win)
For a list of the official rules, visit (https://www.seqanswers.com/forum/sit...wledge-and-win)
See more
See less
X
-
I've noticed that happen on occasion and still haven't really found the cause. My presumption is that the random seeding will be slightly different if you split the files (if the random number generator is always given the same seed, then splitting up a file will result in different numbers being produced if you split reads over files, as opposed to the completely reproducible results if you run an alignment twice). Interestingly, apparently a similar thing happens in BWA if you use different numbers of threads. This was discussed over on Biostars and no one's come up with the base cause yet.
-
Try to further accelerate Bowtie2 alignment
Hi all,
I try to further accelerate Bowtie2 alignment by separating input file to several pieces and using Hadoop-like computing framework to execute.
Based on my understanding, Bowtie2 aligns each pair of read independently.
However, when I separate input files into two parts and merge two outputs of Bowtie2, the content of result file is somewhat not consistent with that of result file generated without separating input.
I would like to ask whether Bowtie2 has some dependent task inside?
Does separating files and then merging the output make sense in Bowtie2?
Thanks.Last edited by Tonnny97; 01-19-2014, 05:15 PM.
Latest Articles
Collapse
-
by seqadmin
Developments in sequencing technologies and methodologies have transformed the field of epigenetics, giving researchers a better way to understand the complex world of gene regulation and heritable modifications. This article explores some of the diverse sequencing methods employed in the study of epigenetics, ranging from classic techniques to cutting-edge innovations while providing a brief overview of their processes, applications, and advances.
Methylation Detect...-
Channel: Articles
05-31-2023, 10:46 AM -
-
Differential Expression and Data Visualization: Recommended Tools for Next-Level Sequencing Analysisby seqadmin
After covering QC and alignment tools in the first segment and variant analysis and genome assembly in the second segment, we’re wrapping up with a discussion about tools for differential gene expression analysis and data visualization. In this article, we include recommendations from the following experts: Dr. Mark Ziemann, Senior Lecturer in Biotechnology and Bioinformatics, Deakin University; Dr. Medhat Mahmoud Postdoctoral Research Fellow at Baylor College of Medicine;...-
Channel: Articles
05-23-2023, 12:26 PM -
-
by seqadmin
Continuing from our previous article, we share variant analysis and genome assembly tools recommended by our experts Dr. Medhat Mahmoud, Postdoctoral Research Fellow at Baylor College of Medicine, and Dr. Ming "Tommy" Tang, Director of Computational Biology at Immunitas and author of From Cell Line to Command Line.
Variant detection and analysis tools
Mahmoud classifies variant detection work into two main groups: short variants (<50...-
Channel: Articles
05-19-2023, 10:03 AM -
ad_right_rmr
Collapse
News
Collapse
Topics | Statistics | Last Post | ||
---|---|---|---|---|
Started by seqadmin, 06-07-2023, 07:14 AM
|
0 responses
11 views
0 likes
|
Last Post
by seqadmin
06-07-2023, 07:14 AM
|
||
Started by seqadmin, 06-06-2023, 01:08 PM
|
0 responses
11 views
0 likes
|
Last Post
by seqadmin
06-06-2023, 01:08 PM
|
||
Started by seqadmin, 06-01-2023, 08:56 PM
|
0 responses
164 views
0 likes
|
Last Post
by seqadmin
06-01-2023, 08:56 PM
|
||
Deep Sequencing Unearths Novel Genetic Variants: Enhancing Precision Medicine for Vascular Anomalies
by seqadmin
Started by seqadmin, 06-01-2023, 07:33 AM
|
0 responses
299 views
0 likes
|
Last Post
by seqadmin
06-01-2023, 07:33 AM
|
Leave a comment: