User: novicebioinforesearcher
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Posts by novicebioinforesearcher
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... will this work just did a bit or more research
> To generate read counts, you must run QoRTs [4] on each aligned bam
> file. QoRTs includes a basic function that calculates a variety of QC
> metrics along with gene-level and splice-junction-level counts. All
> these functions can be pe ...
written 21 months ago by
novicebioinforesearcher • 50
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... So is there any way to do this outside of using those splicing tools? we have curated list of splice junctions that have been seen to change in certain conditions, (around 200 junctions), we did match those 200 with hisat2's script output and now just need reads mapping to it will bedtools perform s ...
written 21 months ago by
novicebioinforesearcher • 50
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... we have RNA seq bam aligned using Hisat2, since hisat provides `hisat2_extract_splice_sites.py` script which gives co ordinates for splice junctions was wondering if some one could point us to how we can obtain reads mapping to these junctions something similar to Htseq where it provides genes mapp ...
written 21 months ago by
novicebioinforesearcher • 50
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... how did u get the code? ...
written 2.2 years ago by
novicebioinforesearcher • 50
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... I have compared 5 different conditions using rMATS, which outputs 5 different files for each alternative splicing event.
I would like to first find a common junctions in skipped exon (Event) across all this 5 conditions(text files) and write the read count and other meta information in a new file, ...
written 2.5 years ago by
novicebioinforesearcher • 50
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... Sure, some additional info about the experiment attempting to detect indels from a panel of clones resulting from CRISPR targeted deletion. Regions around the target were PCR amplified to produce a roughly 150bp amplicon, which was then sequenced with as a PE250 run. ...
written 2.5 years ago by
novicebioinforesearcher • 50
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... Apologies for incomplete information,Yes these were PCR amplicons that were sequenced, I aligned the reads using bwa mem, we were trying to induce a deletion and check if worked by sequencing exon 6 of a particular gene. ...
written 2.5 years ago by
novicebioinforesearcher • 50
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... Thanks, will look in to it where can i find adapter sequences? that have been highlighted in fastqc and what about the seond file that has which I am guessing to be index ...
written 2.5 years ago by
novicebioinforesearcher • 50
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... I received fastq files from core they said they have de multiplexed it but when i ran fastqc i can still see some adapters, attached is figure
![Adapter seq fastqc][1]
My question along with fastq files with names like this
_TAGTCTTG_S7_L001_R1_001.fastq.gz
_TAGTCTTG_S7_L001_R2_001.fas ...
written 2.5 years ago by
novicebioinforesearcher • 50
• updated
2.5 years ago by
Brian Bushnell ♦ 17k
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Comment:
C: Miseq Genomic DNA analysis
... we are working on mouse ...
written 2.5 years ago by
novicebioinforesearcher • 50
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