stringtie | Transcript assembly and quantification for RNA-Seq
kandi X-RAY | stringtie Summary
kandi X-RAY | stringtie Summary
Stringtie employs efficient algorithms for transcript structure recovery and abundance estimation from bulk RNA-Seq reads aligned to a reference genome. It takes as input spliced alignments in coordinate-sorted SAM/BAM/CRAM format and produces a GTF output which consists of assembled transcript structures and their estimated expression levels (FPKM/TPM and base coverage values). For additional StringTie documentation and the latest official source and binary packages please refer to the official website:
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QUESTION
I have a dataset that looks something like this:
...ANSWER
Answered 2021-Dec-19 at 09:00Use:
QUESTION
I have a sample.txt
file like below:
ANSWER
Answered 2020-Nov-16 at 21:08You may use a bracket expression to choose from multiple values:
QUESTION
When I run prepDE.py job exit with the following error. I am using StringTie/2.1.4 with Python/2.7.18. Following is the command I was running (inside ADA cluster)
...ANSWER
Answered 2020-Oct-27 at 15:19This is an educated guess based on the error and the documentation linked:
-i INPUT, --input=INPUT, --in=INPUT
– a folder containing all sample sub-directories, or a text file with sample ID and path to its GTF file on each line [default: . ]
Try invoking the script with
QUESTION
I am unsuccessful in running this small snakemake program for StringTie; the dry-run gives an error of MissingInputException for the "rule stringt", I am unable to understand the issue here since the same directory structures works fine for a different snakemake program.
I have already generated the bam files using "hisat2" and is located in the directory : "/alternate_splice/bam_out/" which is stored as "bamdir".
The snakemake should be able to locate the input file since the names and location are appropriate, however it throws an error every time.
I did look at the pervious snakemake related questions, however could not solve this issue. If anyone can help me out here, it would be great!
...There are 4 samples: for the wildcards, it takes the list from the directory which has the fastq files
ANSWER
Answered 2020-Apr-02 at 08:14As the input you have a variable called tname
which isn't used, and I think it is there by mistake:
QUESTION
I have a table in which the header is the sample list and the first column is the gene list, and the rest is expression values for each gene in each sample. I want to add a pseudocount of 1 to all values, and I currently do it as such:
...ANSWER
Answered 2020-Mar-29 at 15:09awk
is great language. Just iterate over fields and increment them.
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