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* Table of Contents :TOC:noexport:
- [[#what-is-the-public-sequence-resource-about][What is the 'public sequence resource' about?]]
+ - [[#presentations][Presentations]]
- [[#who-created-the-public-sequence-resource][Who created the public sequence resource?]]
- [[#how-does-the-public-sequence-resource-compare-to-other-data-resources][How does the public sequence resource compare to other data resources?]]
- [[#why-should-i-upload-my-data-here][Why should I upload my data here?]]
@@ -17,21 +18,54 @@
- [[#how-do-i-change-the-work-flows][How do I change the work flows?]]
- [[#how-do-i-change-the-source-code][How do I change the source code?]]
- [[#should-i-choose-cc-by-or-cc0][Should I choose CC-BY or CC0?]]
- - [[#are-there-also-variant-in-the-RDF-databases]][Are there also variant in the RDF databases?]
+ - [[#are-there-also-variant-in-the-rdf-databases][Are there also variant in the RDF databases?]]
- [[#how-do-i-deal-with-private-data-and-privacy][How do I deal with private data and privacy?]]
- - [[#do-you-have-any-checks-or-concerns-if-human-sequence-accidentally-submitted-to-your-service-as-part-of-a-fastq][Do you have any checks or concerns if human sequence accidentally submitted to your service as part of a fastq?]
- - [[#does-PubSeq-support-only-SARS-CoV-2=data]][Does PubSeq support only SARS-CoV-2 data?]
+ - [[#do-you-have-any-checks-or-concerns-if-human-sequence-accidentally-submitted-to-your-service-as-part-of-a-fastq-][Do you have any checks or concerns if human sequence accidentally submitted to your service as part of a fastq? *]]
+ - [[#does-pubseq-support-only-sars-cov-2-data][Does PubSeq support only SARS-CoV-2 data?]]
- [[#how-do-i-communicate-with-you][How do I communicate with you?]]
+ - [[#citing-pubseq][Citing PubSeq]]
- [[#who-are-the-sponsors][Who are the sponsors?]]
* What is the 'public sequence resource' about?
-The *public sequence resource* aims to provide a generic and useful
-resource for COVID-19 research. The focus is on providing the best
-possible sequence data with associated metadata that can be used for
-sequence comparison and protein prediction.
-
-We were at the *Bioinformatics Community Conference 2020*! Have a look at the [[https://bcc2020.sched.com/event/coLw]][video talk] ([[https://drive.google.com/file/d/1skXHwVKM_gl73-_4giYIOQ1IlC5X5uBo/view?usp=sharing]][alternative link]) and the [[https://drive.google.com/file/d/1vyEgfvSqhM9yIwWZ6Iys-QxhxtVxPSdp/view?usp=sharing]][poster].
+PubSeq, the *public sequence resource*, aims to provide a generic and
+useful resource for COVID-19 research. The focus is on providing the
+best possible sequence data with associated metadata that can be used
+for sequence comparison and protein prediction.
+
+Just to avoid the notion that PubSeq is a biorepository: it is far
+more than that. We are not competing with the likes of GenBank,
+EBI/ENA and GISAID - in fact, PubSeq sources much of the data from
+those and they get ours.
+
+There is no conflict of posting data to multiple repositories.
+
+It is better to view PubSeq as an *open precision medicine initiative* that
+allows for early detection of new variants and strains; very valuable
+for both testing and treatment. We have live analysis work flows that
+run on uploading a new sequence. Contributing sequences helps the
+overall detection. At this moment the output is limited. We will soon
+add interactive discovery tools. Uploading data from a sequencer will
+give researchers all information they want in 5 hours *without any
+bioinformatics knowledge*. We may even provide workflows that take
+data straight from the sequencer. In fact, you get very little out of
+existing biorepositories, in our opinion, unless you have solid
+bioinformatics support. And even then there is the question about
+comparing data that was created using different technologies and
+workflows. How do you deal with that?
+
+With PubSeq we are in a position to reanalyse that data from raw
+material when new insights arise. It is likely that COVID19 will be
+around for another year at least. After that we should prepare for
+the next pandemic. PubSeq is meant for that. We take the long view and
+it will only get more powerful. Who knows: maybe the live analysis
+part of PubSeq will be an approach that other biorepositories will
+follow.
+
+* Presentations
+
+We presented at the BOSC 2020 Have a look at the [[https://bcc2020.sched.com/event/coLw][video]] ([[https://drive.google.com/file/d/1skXHwVKM_gl73-_4giYIOQ1IlC5X5uBo/view?usp=sharing][alternative
+link]]) and the [[https://drive.google.com/file/d/1vyEgfvSqhM9yIwWZ6Iys-QxhxtVxPSdp/view?usp=sharing][poster]].
* Who created the public sequence resource?
@@ -176,7 +210,7 @@ because we know people like the attribution clause.
In all honesty: we prefer both data and software to be free.
-* Are there also variant in the RDF databases? *
+* Are there also variant in the RDF databases?
We do output a RDF file with the pangenome built in, and you can parse it because it has variants implicitly.
@@ -193,14 +227,23 @@ plan to combine identifiers with clinical data stored securely at
We are planning to remove reads that match the human reference.
-* Does PubSeq support only SARS-CoV-2 data? *
+* Does PubSeq support only SARS-CoV-2 data?
To date, PubSeq is a resource specific to SARS-CoV-2, but we are designing it to be able to support other species in the future.
* How do I communicate with you?
-We use a [[https://gitter.im/arvados/pubseq?utm_source=share-link&utm_medium=link&utm_campaign=share-link][gitter channel]] you can join.
+We use a [[https://gitter.im/arvados/pubseq?utm_source=share-link&utm_medium=link&utm_campaign=share-link][gitter channel]] you can join. See also [[./contact][contact]].
+
+* Citing PubSeq
+
+We have two publications in the works. Until we have a DOI please cite
+PubSeq in the following way:
+
+We made use of the COVID-19 public sequence (PubSeq) resources hosted
+at http://covid19.genenetwork.org/.
+
* Who are the sponsors?