deepcelllineage / deepcelllineage/mitolin
Annotate mitochondrial DNA fasta files with genes
- Dominant language
- Jupyter Notebook
- Stars
- 2
- Forks
- 4
- PR merge metrics
- No merged PRs in 30d
Description
## Aim
Annotate the gene features of mitochondrial DNA.
## Background
Gene annotation will allow us to tokenize the mitochondria sequences smarter. We will do this on the small (16,000 nt) mitochondria DNA first. This will lay the groundwork for annotating all expressed mRNA genes and even later in the project the whole genome.
In [slides in overview/wiki](https://github.com/deepcelllineage/overview/wiki/slides), see Science #1 slides for the difference between mitochondria and nuclear DNA and (on slide 4) an image of the 13 proteins, 22 tRNA, 2 rRNA, and D-loop whose coordinates we want to annotate.
## Method
The software [Annovar](http://annovar.openbioinformatics.org/en/latest/) was recommended as a good starting place by Kerrigan Blake, a PhD student in the Lawson Lab.
You could also search google with phrases like "annotate genes software packages free" or "SciPy gene annotation" to find what package would be best.
## Data
Nine 19KB files are here:
deepcelllineage/data01/gen/nguyen_nc_2018/20190710-320lfastas/
(data01 is a separate repo within deepcelllineage)
A link to the nine files is here:
https://github.com/deepcelllineage/data01/tree/master/gen/nguyen_nc_2018/20190710-320lfastas
These are .fasta files that are the full length of the mitochondrial gene plus some of chr1. There is a separate issue to chop off the chr1 part.
I used `for f in *; do grep -n ">2" $f; done` to check that each goes into chr1.
## Document your work
Please fork & clone this repo. Check out a branch for your work, then push and make a PR for us to merge your note and files.
Add a note (can be .md or .ipynb) with your solution to [mitolin/nb](https://github.com/deepcelllineage/mitolin/tree/master/nb).
Your note should be named as follows:
- DATE-issue#-shortdescription.ext
e.g.:
- 20190701-i02-extract-chrM-fa.md
## Questions?
Please put questions related to this issue in this issue thread.
If you want a quick response, post a link to your comment in this thread to Slack #deepcelllineage and tag @Deena or others. You can also DM @Deena.
To join Slack enter your email address [here](http://bit.ly/JoinSlackFastaiSFbay). For questions NOT specifically related to this issue, get in touch through any of the communication methods listed in [DCL's overview README](https://github.com/deepcelllineage/overview/blob/master/README.md).
Contributor guide
No contributing guide indexed for this repository
Research direction
Start with the Science #1 overview slides and the nine FASTA files in data01/gen/nguyen_nc_2018/20190710-320lfastas/, then evaluate Annovar or another suitable annotation package. Record the approach and results in a dated .md or .ipynb note under mitolin/nb, and include the annotated mitochondrial gene features and any relevant files in a pull request.
Written by the indexing model from the issue text.
Assessment
- Tech stack
- jupyter-notebook
- Domain
- bioinformatics, data
- Issue type
- Feature
- Difficulty
- 4/5
- Estimated time
- 3-5 days
- Activity status
- Stale
- Clarity
- Mostly clear
- Newbie friendliness
- 35/100