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Hi,
I'm attempting to align paired-end RNAseq data, which I previously trimmed using trimgalore, with STAR. STAR, however, is not finding the fastq files.
Here is my batch script:
R1=/projec…
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**dear author, sorry to disturb you, but it seems something wrong with the reassemble_bin module. when I use the pipeline, finally i got the result but, the contamination of reassembled bins (bin.stri…
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Hi,
`finch dist`, `finch hist` and `finch info` do not work on sketch files that do not end with `.sk`
**With suffix:**
```bash
finch sketch ecoli*
finch dist ecoli*.sk
# [{"containment":…
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Allow searching by place name to take user to the location of that place
Make use of the API which powers https://placenames.fsdf.org.au/
EG, searching for Kanangra Boyd NP location.
**Input1…
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Die API könnte auf jeder Seite Kontext-spezifisch "promoted" werden. Dazu könnte jeweils ein Kasten mit dem Link zu API-Anfrage, welche die gerade angezeigte Abfrage repräsentiert, eingebunden werden.…
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## Environment
- Android OS version: Android 12
- Devices affected: Only Samsung devices (SM-S908U, SM-G996U, SM-S901U, SM-N986U, SM-F711U, SM-F936U, ...)
- Maps SDK Version: 10.7.0, 10.8.0
##…
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I used HIFI and HIC data to assembly a genome(~3Gb), command: hifiasm -o Y_asm -t 70 --h1 ../HIC/*_1.fq.gz --h2 ../HIC/*_2.fq.gz ../01.ccs/HiFireads/*.subreads.fastq.gz. But i can't understand what is…
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Can not detect the fusions with the test data,is anyone can help me? all the testdata is from the git and
http://opengene.org/dataset.html
Here is my shell command:
./genefuse -r Homo_sapiens_a…
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Found something interesting this morning working with string types. The field is indexed as such:
``` ruby
string :board_specialty, :multiple => true do
user.certifications.map(&:specialty) if user…
brupm updated
7 years ago
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hi,doctor
i encounter a problem when use hisat2 ,can you give me some advice
fisrt,i use hisat2 build index for a large genome : hisat2-build --large-index ,it doesn't report any error .
…