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feat: content for the roadmap page (#93)
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Fran McDade
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Fran McDade
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app/components/Roadmap/components/Section/components/SectionRoadmap/sectionRoadmap.styles.ts
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app/components/Roadmap/components/Section/components/SectionRoadmap/sectionRoadmap.tsx
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app/components/Roadmap/components/Section/components/SectionSubhero/sectionSubhero.styles.ts
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app/components/Roadmap/components/Section/components/SectionSubhero/sectionSubhero.tsx
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export { default as SectionAbout } from "./sectionAbout.mdx"; | ||
export { default as SectionRoadmap } from "./sectionRoadmap.mdx"; |
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<Section border> | ||
<SectionLayout paired> | ||
<SectionHeadline paired> | ||
## Our plan | ||
<SubHeadline> | ||
This will be an iterative process involving multiple steps in several | ||
areas: | ||
</SubHeadline> | ||
</SectionHeadline> | ||
<SectionContent paired> | ||
<Grid gridSx={{ gap: 4 }}> | ||
<Accordion> | ||
<AccordionSummary>VEuPathDb database migration</AccordionSummary> | ||
<AccordionDetails> | ||
This set of tasks deals with transferring data from VEuPathDb | ||
infrastructure and creating a list of genomes that will be initially | ||
maintained within BRC-Analytics. The number of taxa included in our | ||
system will | ||
|
||
1. Transferring databases and associated data from VEuPathDb servers to TACC infrastructure. | ||
1. Understanding the structure of VEuPathDb database and deciding which data will be ingested as custom | ||
tracks for the BRC-analytics instance of the UCSC Genome Browser. | ||
1. Uncovering how JBrowse instances were created within VEuPathDb gene pages and replicating this data at | ||
the BRC-analytics instance of the UCSC Genome Browser. | ||
</AccordionDetails> | ||
</Accordion> | ||
<Accordion> | ||
<AccordionSummary>Harmonization of genomic data for all taxa</AccordionSummary> | ||
<AccordionDetails> | ||
This set of tasks ensures that BRC-analytics provides access to the latest versions of all 785 VEuPathDb | ||
taxa and associated annotations. | ||
|
||
1. Build UCSC Genome Browsers for all 785 taxa by matching genomes found in VEuPathDb against NCBI Datasets. | ||
1. Add annotations that can be extracted from the VEuPathDb databases and JBrowse instances (related to 2 | ||
and 3 above) | ||
1. Create links from UCSC Gene Pages to NCBI Gene pages | ||
1. Work with NCBI on evolution of gene pages to contain information similar to what was contained within the | ||
VEuPathDb gene pages. | ||
</AccordionDetails> | ||
</Accordion> | ||
<Accordion> | ||
<AccordionSummary>Galaxy integration</AccordionSummary> | ||
<AccordionDetails> | ||
1. Create a dedicated Galaxy instance at [https://brc.usegalaxy.org](https://brc.usegalaxy.org) | ||
1. Prepare reference data for all 785 genomes that will initially be served by the system. This includes | ||
creation of indices for bowtie, bowtie2, bwa-mem, bwa-mem2, hisat2, STAR, and SnpEff. | ||
1. Create a single sign-on so that user accounts are shared between brc-analytics and Galaxy. When creating | ||
an account the user should be able to specify the default Galaxy instances (.org, .eu., .org.au, .fr ...) | ||
1. Develop functionality for "focusing" Galaxy on a particular genome build selected by the user (see | ||
["Focusing" Galaxy on a particular genome | ||
galaxy#18882](https://github.com/galaxyproject/galaxy/issues/18882)). | ||
1. Develop "simplified workflow" interface (see [Simplified workflow run interface | ||
galaxy#18883](https://github.com/galaxyproject/galaxy/issues/18883)) | ||
1. Develop and polish workflows for variant discovery, epigenetics, transcriptomics, assembly, and protein | ||
folding that were previously available to the users on VEuPathDb Galaxy instance. | ||
</AccordionDetails> | ||
</Accordion> | ||
<Accordion> | ||
<AccordionSummary>Help and community outreach</AccordionSummary> | ||
<AccordionDetails> | ||
1. Create dedicated linkedin, mastodon, and bluesky accounts | ||
1. Create a dedicated support channel using Discourse infrastructure. | ||
1. Try to connect with as many users of VEuPathDb as possible to solicit their feedback across multiple | ||
areas including: which features are needed, what genomes should be integrated, which key datasets need to be | ||
re-analyzed in put in the context of available genomic data. | ||
1. Beginning on Oct 1st begin posting regular updates via social media channels. | ||
</AccordionDetails> | ||
</Accordion> | ||
</Grid> | ||
</SectionContent> | ||
|
||
</SectionLayout> | ||
</Section> |
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