User: stacy734
stacy734 • 40
- Reputation:
- 40
- Status:
- New User
- Location:
- Last seen:
- 1 month, 3 weeks ago
- Joined:
- 3 years, 2 months ago
- Email:
- s*******@yahoo.com
Posts by stacy734
<prev
• 27 results •
page 1 of 3 •
next >
0
votes
4
answers
239
views
4
answers
... Thank you everyone.
This request was to help with submission of genome assemblies to Genbank. They ask that the terminal Ns (gaps) be removed from the ends of contigs. However, I have found that if you simply leave them on they will remove them as part of their process. ...
written 9 weeks ago by
stacy734 • 40
2
votes
4
answers
239
views
5 follow
4
answers
... Can anyone recommend a tool or unix command line to remove terminal (leading or trailing) Ns from a fasta file?
Thanks in advance for any advice. ...
written 9 weeks ago by
stacy734 • 40
0
votes
0
answers
180
views
0
answers
... I have Spades running on a compute farm with 500G RAM. It is still running and only using 310G of the RAM allowed.
There is plenty of disk space (~4 TB).
I'll just let it roll.
Thanks for your comments! ...
written 3 months ago by
stacy734 • 40
0
votes
0
answers
180
views
0
answers
... Hi all,
I am running a genome assembly using Spades on a 1GB genome using ~120GB paired-end Illumina reads.
The process has been running for more than a week, mostly on the K-mer counting step. The log shows a notation : "Collecting K-mer information, this takes a while" so maybe this is expecte ...
written 3 months ago by
stacy734 • 40
0
votes
0
answers
166
views
0
answers
... Hi all,
Does anyone know if the SPAdes assembler loses singlets (unassembled strings)? In other words, if it is run on partially assembled deduped genome, will it lose all contigs that can't be further joined?
Thanks for any advice. ...
written 5 months ago by
stacy734 • 40
0
votes
0
answers
194
views
0
answers
... Hi everyone,
I recently submitted an insect genome to Genbank, and received back a very helpful report showing some contigs had contaminating bacteria. Most of this was removed prior to submission by Blasting against the bacterial db, but it looks like some were missed.
Does anyone know how to ge ...
written 7 months ago by
stacy734 • 40
0
votes
1
answer
1.8k
views
1
answers
Comment:
C: Oxford Nanopore error rate?
... Thank you WouterDeCoster for posting this image.
Can you post the title of the paper? I'd like to read it for more details. ...
written 9 months ago by
stacy734 • 40
0
votes
1
answer
1.8k
views
1
answers
Comment:
C: Oxford Nanopore error rate?
... No, sadly there is no reference genome available. This would be for de novo assembly. ...
written 9 months ago by
stacy734 • 40
4
votes
1
answer
1.8k
views
1
answer
... I'm considering trying the Oxford Nanopore sequencer.
I know at one point they had a very high error rate, which they advertise as being much lower now. I'm looking for a recent paper from an unbiased source that has tested what the error rate is in a real world process.
I have emailed the compa ...
written 9 months ago by
stacy734 • 40
• updated
9 months ago by
WouterDeCoster ♦ 43k
0
votes
2
answers
330
views
2
answers
Answer:
A: Advice on Blast output
... Thanks!
For others who may read this, the parameter in question can either be sskingdom or sblastname.
Stacy ...
written 12 months ago by
stacy734 • 40
Latest awards to stacy734
Popular Question
4 months ago,
created a question with more than 1,000 views.
For Question about k-mer genie output
Popular Question
7 months ago,
created a question with more than 1,000 views.
For Exporting fasta from SQL
Popular Question
12 months ago,
created a question with more than 1,000 views.
For Question about k-mer genie output
Use of this site constitutes acceptance of our User
Agreement
and Privacy
Policy.
Powered by Biostar
version 2.3.0
Traffic: 2082 users visited in the last hour