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A: Extracting reads with low mapping score from Bam file
A: Samtools mpileup of soft-clipped alignment behaves non-deterministically?
Answer: convert .bed format to .txt format
Answer: convert .bed format to .txt format
Answer: Extract nucleotide sequence from a RefSeq Transcript ID
Answer: Extract nucleotide sequence from a RefSeq Transcript ID
Answer: R - cleanest way to calculate mean of a columnX in dataset1, columnZ in dataset2
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Answer: Stringtie skips some reference genes
by
Antonio R. Franco
★ 4.9k
If using RNA, I would expect not having the complete set of genes being expressed
Comment: convert .bed format to .txt format
by
rheab1230
▴ 60
Yes, I was able to view it. Thank you.
Comment: Extract nucleotide sequence from a RefSeq Transcript ID
by
Vincent Laufer
★ 2.2k
thank you!!!!!!!!!!! this was so helpful. makes me think we convenient browser based tools etc. i really appreciate you.
Answer: Extract nucleotide sequence from a RefSeq Transcript ID
by
GenoMax
118k
Using [**Entrezdirect**][1]. Example for getting nucleotides 1101 to 1120. $ efetch -db nuccore -id NM_001346941.2 -seq_start 1101 -se…
Comment: Using whole exome data from different protocols
by
m.bamajboor
• 0
I have similer question regarding the kits used for sequencing. I'm in a process of calculating the allele frequency of a group of samples,…
Comment: vcf2maf allele frequency not converting
by
hamrejr
• 0
Thanks. I am trying to get this on the maf from the vcf. So the command I am using is: vcf2maf.pl --input-vcf .vcf --output-maf .vcf.m…
Comment: [RNAseq, featureCounts] Can paired-end data be processed as single end?
by
Luka
• 0
The IDs were indeed a problem, the processing worked after changing them. Thanks for all the help!
Answer: vcf2maf allele frequency not converting
by
Pierre Lindenbaum
147k
not tested but that could be: paste <(bcftools view in.vcf | grep -v "^#") <(bcftools query -f '%INFO/AF\n' in.vcf)
Comment: Cannot install ATHLATES, issues with bamtools
by
gogo21
• 0
yeah I am also getting the same issue is this issue due to wrong path provided ?
Comment: Dual index barcode demultiplex issue
by
BioRyder
▴ 220
Hello @devon / John Marshall We have noticed some exceptional cases in our recent Novaseq run. We were using 'Dual Index Bio Scientific-…
Comment: R - cleanest way to calculate mean of a columnX in dataset1, columnZ in dataset2
by
Bianca
• 0
I found out why. I was loading plyr after dplyr, that was my problem. I removed library(plyr) from my code and only loaded (dplyr). Now it …
Answer: merging data; remove extra rows
by
swbarnes2
12k
Is this RSEM format? Or some other format that txinport can handle?
Comment: R - cleanest way to calculate mean of a columnX in dataset1, columnZ in dataset2
by
Bianca
• 0
Hello, that did not work. It returned the mean value of all the data frames combined and the sum of all the data frames combined. It return…
Comment: What is the best way to rank genes for GSEA?
by
hermidalc
▴ 20
Just because you see something in published papers doesn't mean it's good or recommended, a lot of authors miss things or do not have a dee…
Comment: Cannot call haplotypes on bam
by
Shred
▴ 730
Sure. Use bwa instead
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