Forum: Bioinformatics
10-02-2019, 02:53 AM
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Replies: 3
Views: 1,415
Personally, I would do quality and adapter...
Personally, I would do quality and adapter trimming (and maybe error-correction) of the raw Illumina reads as MaSuRCA pretty much does this from what I understand and use the quality and adapter...
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Forum: Bioinformatics
09-03-2019, 11:18 PM
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Replies: 1
Views: 1,192
I would call SNPs with your desired variant...
I would call SNPs with your desired variant caller (I prefer CallVariants from BBTools/BBMap) then use bedtools intersect (-a study.vcf.gz -b bed-file-of-snps) and the output is a VCF file of...
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Forum: Bioinformatics
09-02-2019, 01:42 AM
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Replies: 2
Views: 1,044
No this is not common, but MAKER's...
No this is not common, but MAKER's (http://www.yandell-lab.org/software/maker.html) gff3_merge script can output a GFF file with FASTA sequence at the end.
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Forum: Bioinformatics
05-02-2019, 04:23 AM
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Replies: 2
Views: 1,526
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Forum: Bioinformatics
04-28-2019, 11:09 PM
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Replies: 1
Views: 1,206
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Forum: RNA Sequencing
04-15-2019, 04:38 AM
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Replies: 3
Views: 2,725
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Forum: Bioinformatics
04-09-2019, 12:26 AM
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Replies: 1
Views: 889
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Forum: Illumina/Solexa
03-12-2019, 11:33 PM
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Replies: 3
Views: 924
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Forum: Bioinformatics
12-04-2018, 02:53 AM
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Replies: 1
Views: 1,021
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Forum: Bioinformatics
11-13-2018, 10:23 PM
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Replies: 5
Views: 1,762
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Forum: Bioinformatics
11-12-2018, 01:35 AM
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Replies: 5
Views: 1,762
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Forum: Bioinformatics
11-07-2018, 02:47 AM
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Replies: 5
Views: 1,762
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Forum: Pacific Biosciences
10-27-2018, 03:56 AM
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Replies: 5
Views: 3,414
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Forum: Pacific Biosciences
10-22-2018, 10:13 PM
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Replies: 5
Views: 3,414
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Forum: Pacific Biosciences
10-20-2018, 05:53 AM
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Replies: 5
Views: 3,414
For the PacBio Sequel data, were you using the...
For the PacBio Sequel data, were you using the raw subreads? That's what I would recommend. By default the PacBio subread BAM files give a quality score of Q0 to all bases, and PBJelly needs quality...
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Forum: Bioinformatics
08-08-2018, 10:11 PM
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Replies: 4
Views: 3,254
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Forum: Bioinformatics
08-07-2018, 02:58 AM
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Replies: 4
Views: 3,254
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Forum: Bioinformatics
04-26-2018, 09:35 PM
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Replies: 679
Views: 217,708
Hi Brian,
Does bbmap callvariants.sh ignore...
Hi Brian,
Does bbmap callvariants.sh ignore duplicates marked by picard MarkDuplicates by default (or is there an option to ignore duplicates) or do duplicates have to be deleted?
Best,
Gopo
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Forum: Bioinformatics
02-11-2018, 09:56 PM
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Replies: 3
Views: 1,757
So, I had this problem- it could be due to two...
So, I had this problem- it could be due to two things:
(1) By default BUSCO has a file called /path-to-busco-installation/busco/config/config.ini.default. That file needs to modified and renamed as...
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Forum: Genomic Resequencing
02-04-2018, 02:06 AM
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Replies: 2
Views: 6,788
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Forum: General
01-23-2018, 11:11 AM
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Replies: 3
Views: 1,730
Unfortunately, I can't really give too much...
Unfortunately, I can't really give too much advice about optimizing. Others on the forum have more experience than I do. I've personally subsampled a dataset of 16 individuals, 4 per population,...
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Forum: General
01-23-2018, 10:43 AM
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Replies: 3
Views: 1,730
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Forum: Bioinformatics
01-23-2018, 12:15 AM
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Replies: 39
Views: 33,965
I am not sure this is a bug or not, but when I...
I am not sure this is a bug or not, but when I try to use reformat.sh (version 37.76) to add fake qualities of Q30 to a PacBio Sequel fastq file (produced with bamtools convert -format fastq -in...
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Forum: Bioinformatics
11-02-2017, 06:30 AM
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Replies: 104
Views: 42,196
Hi Brian,
I recreated the paired-end FASTQ...
Hi Brian,
I recreated the paired-end FASTQ files, performed adapter and quality trimming with bbduk, then used tadpole for error correction, and finally used tadpole in contig mode to de novo...
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Forum: Bioinformatics
10-13-2017, 12:49 PM
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Replies: 104
Views: 42,196
Hi Brian,
I used bbmerge and am now trying...
Hi Brian,
I used bbmerge and am now trying to error correct my paired and merged reads with tadpole at the same, but I can't seem to get the right syntax for the input
I tried the following...
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