Comments (3)
The issues have been fixed.
from biostar-handbook.
Just a small follow up on the issue:
The text after the fixed link in Variant effect prediction is not correct as it states that the script needs to be edited to modify the accession number. The accession number is given as a parameter on the command line so no editing is needed.
In addition, for running the annotation after the script the command snpEff ebola_zaire samples.vcf > annotated.vcf is suggested. The script will produce a vcf file for each run and one for all runs combined: SRR19729[17,18,19,20,21].vcf and combined.vcf. None is called samples.vcf. It is quite obvious what is meant but may be confusing for a newbie trying to learn.
from biostar-handbook.
Indeed, inconsistencies do creep in. Thanks for reporting. The changes have been made.
from biostar-handbook.
Related Issues (20)
- A problem in running "How to install software" HOT 1
- Failed at Step 9 of Step-by-Step installation HOT 2
- Introduction to taxonomies HOT 1
- "samtools sort" command is not working HOT 2
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- Using Windows 10 for the script
- Mamba Installation (xargs: mamba: no such file or directory) HOT 2
- Workflows: Update for install step (src/hisat2.mk, src/fastp.mk, src/salmon.mk) HOT 1
- installation issue HOT 4
- Installation of miniconda HOT 12
- install software: run a realistic analysis HOT 1
- Extremely minor nitpicky issue: Sublime Text 2 is now Sublime Text 4 HOT 1
- Fail to install bioinformatics software
- A typo in the chapter "Classifying whole genome data"
- Missing Apple Silicon (ARM) support in install.sh HOT 7
- Issues in find-variants.sh HOT 3
- Stuck at Doctor.py step for installation process HOT 6
- install issue with quick install command HOT 13
- gunzip hg38.knownGene.gtf.gz not in gzip format HOT 1
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from biostar-handbook.