Hello all,
After some thought we've decided to add a couple of names to the author list of the LoF abstract.
Our initial author list included people who are contributing specifically to
LoF analysis, Natalja and Thasso for processing of the entire dataset,
and the PIs and the Geuvadis Consortium representing the data.
But it's fair to include one analysis person from all the labs on behalf of the data production, so we added Marc, Matthias, Olof, and Monkol from Daniel's lab.
Thus, the latest version of the author list is the following:
Manuel A Rivas, Tuuli Lappalainen, Michael Sammeth, Daniel MacArthur, Natalja Kurbatova, Thomas Wieland, Monkol Lek, Thasso Griebel, Matthias Barann, Marc Sultan, Olof Karlberg, Peter AC ‘t Hoen, Tim Strom, Stefan Schreiber, Hans Lehrach, Stylianos Antonarakis, Gert-Jan van Ommen, Ralf Sudbrak, Robert Häsler, Alvis Brazma, Ann-Christine Syvanen, Philip Rosenstiel, Thomas Meitinger, Roderic Guigo, Ivo Gut, Xavier Estivill, Mark McCarthy, Emmanouil T Dermitzakis, The Geuvadis Consortium
best regards,
Tuuli
Le 01-06-12, Manuel Rivas <rivas(a)broadinstitute.org> a écrit :
> Hello,
>
> Attached is an abstract that I am planning to submit on behalf of the project on loss of variants and their effect on the transcriptome. Please do send any comments you may have by Monday, June 4th.
>
>
>
>
> Best Regards,
> Manuel Rivas
>
>
>
Hello,
Attached is an abstract that I am planning to submit on behalf of the
project on loss of variants and their effect on the transcriptome. Please
do send any comments you may have by Monday, June 4th.
Best Regards,
Manuel Rivas
Dear all,
Enclosed please find a draft for the abstract that I'm planning to
submit on behalf of the Geuvadis RNAseq project for the ASHG meeting in
San Francisco. Comments are welcome; please send them by June 4th.
The abstract has the maximum allowed number of authors (30) - at least
one analyst per group and the PIs. I know there are many others who
would deserve to be on that list, and apologies for not being able to
include you here.
In addition to this main abstract, there will be at least one
sub-project abstract that will be sent around later.
best regards,
Tuuli
--
Tuuli Lappalainen, PhD
Department of Genetic Medicine and Development
University of Geneva Medical School
CMU / Rue Michel-Servet 1
1211 Geneva 4
Switzerland
Tel. +41-(0)22-3795550
tuuli.lappalainen(a)unige.ch
Dear all,
Please find here the registration form<https://docs.google.com/spreadsheet/viewform?pli=1&formkey=dDFxZ2diT0hUVFhu…> for the 2nd GEUVADIS RNA analysis meeting; which will take place at the CRG in Barcelona; on:.
Monday July 9th; from 12:00 to 17:00
Tuesday July 10th; from 09:00 to 16:00.
A detail agenda will follow soon.
Please forward this to any relevant person in your lab.
Registration deadline: 8th June 2012
The hotel has to be paid from your own GEUVADIS budget.
We have pre-booked 30 hotel rooms for the 9th of July near the CRG; in:
Hotel H10 Marina<http://www.hotelh10marinabarcelona.com/en/index.html>
Hotel H4<http://www.besthotelscities.com/hotel4barcelona/index.php>
If you want to stay for more nights, or in a different hotel please tick the according box in the registration form, and we'll provide you with hotel suggestions.
Registration form full link: https://docs.google.com/spreadsheet/viewform?pli=1&formkey=dDFxZ2diT0hUVFhu…
Don't hesitate to contact me in case you have any question,
Kind regards,
Gabrielle
Gabrielle Bertier
Scientific Project Manager
International and Scientific Affairs
CRG, Center for Genomic Regulation
Carrer Dr. Aiguader, 88
08003 Barcelona, España
Tel: +34933160374
Mobile: +34639960656
email: gabrielle.bertier(a)crg.es<mailto:gabrielle.bertier@crg.es>
web: www.geuvadis.eu; www.fliact.eu
Hello all,
I'd like to update to Gencode v12 gene annotation (Ensembl 67) in the
Geuvadis RNAseq project after all.
After a lot of discussions, I'm now taking back my last week's decision
to stick to v7. That would have made some things easier but others more
difficult, and I wouldn't want us to lose any power because of an
outdated annotation that might make a bit of a difference especially in
the LoF variant annotations. It's not too late to switch yet - we'll
need to rerun the transcript quantifications though. We'll let you know
when it's done. No one expressed a strong opinion about this before, but
if you disagree, please say it now.
best regards,
Tuuli
--
Tuuli Lappalainen, PhD
Department of Genetic Medicine and Development
University of Geneva Medical School
CMU / Rue Michel-Servet 1
1211 Geneva 4
Switzerland
Tel. +41-(0)22-3795550
tuuli.lappalainen(a)unige.ch
Dear all,
Bam files from GEM are now available for download in
/upload/geuvadis/wp4_rnaseq/main_project/sequence_data/bam/mrna/gem/ .
These are big files so I strongly recommend using aspera; the command
for downloading all the files of that folder would be like:
cd /my/dir/for/geuvadis/bam/
~/.aspera/connect/bin/ascp -QT -l 150M -k1
geuvadis@ah01.ebi.ac.uk:/upload/geuvadis/wp4_rnaseq/main_project/sequence_data/bam/mrna/gem/
.
(this would create a folder gem/ in /my/dir/for/geuvadis/bam/ and
download the files there. -k1 means that it will automatically skip
downloading a file again if the name and size matches, which is very
useful when you need to restart a download)
best regards,
Tuuli
--
Tuuli Lappalainen, PhD
Department of Genetic Medicine and Development
University of Geneva Medical School
CMU / Rue Michel-Servet 1
1211 Geneva 4
Switzerland
Tel. +41-(0)22-3795550
tuuli.lappalainen(a)unige.ch
Hello all,
We'll have a Geuvadis analysis group TC today (May 24th) at 2pm CET.
On the agenda:
- ASHG abstract(s)
- wiki and shared writing tools
- plans for public sharing of data and documentation
- data formats and identifiers
- variant annotations
- Manny will give an update of LoF analysis
- Tuuli will present some slides of ASE analysis (if there's time)
Call details are:
from outside spain; 0034917911859
from spain; 900800678
Access code; 3160100
best regards,
Tuuli
--
Tuuli Lappalainen, PhD
Department of Genetic Medicine and Development
University of Geneva Medical School
CMU / Rue Michel-Servet 1
1211 Geneva 4
Switzerland
Tel. +41-(0)22-3795550
tuuli.lappalainen(a)unige.ch
Hello all,
I've written some updates in the Geuvadis wiki:
- I've created a page for identifier and file format information. We
will all have less grey hair by the end of the project if we are
consistent on these things. Please go and update those parts of data
that concern you, and let people know of changes also by email - and
check this page when creating data files!
http://www.geuvadis.org/group/geuvadis/wikis/-/wiki/Main%20Geuvadis%20Wiki/…
- I wrote quite a lot of text about ASE analysis - background
information, summary of our pipeline, potential sources of error,
available data, and a list of analysis that I'll keep on updating with
results later on.
http://www.geuvadis.org/group/geuvadis/wikis/-/wiki/Main%20Geuvadis%20Wiki/…
best regards,
Tuuli
--
Tuuli Lappalainen, PhD
Department of Genetic Medicine and Development
University of Geneva Medical School
CMU / Rue Michel-Servet 1
1211 Geneva 4
Switzerland
Tel. +41-(0)22-3795550
tuuli.lappalainen(a)unige.ch
Dear all,
we just replaced the transcript quantification files in
analysis_data/quantification/transcript because we found that a script
which counted the number of mapped reads for the RPKM normalization
got confused by the whitespace characters inserted by the new
casava/Illumina pipeline into the read IDs. Therefore, the RPKM values
in the former files were off by ~ factor 2, the exact ratio old/new
varies expectedly few % around the median 1.92 (plot attached).
Hopefully this lapsus did not affect anybody's work--and please be
careful not to run into the same issue when emplyoing programs that
split columns by whitespaces on files with these read IDs; that was
really a great idea of Illumina.
Best,
micha
--
Dr. Michael Sammeth, GL Functional Bioinformatics
Phone: +34-934-020-580, http://www.cnag.eu
Centre Nacional d'Anàlisi Genòmica (CNAG), PCB
Baldiri Reixac 4-6, Room 02A8, 08028 Barcelona
Hi all - especially Thasso and Micha,
In order to correct/filter for allelic mapping bias in Geuvadis analysis
as we've discussed before, I've simulated reads over 1000g variants.
The fastq files are available for mapping in
/upload/geuvadis/wp4_rnaseq/main_project/external_data/genetic_variation/allelic_mapping_simulation/fastq
. These should be mapped with GEM and converted to bam similarly to our
real data, except that these are single-end reads. It actually became a
lot less reads than I anticipated because I ended up taking only sites
that are polymorphic in our populations: it's about 300M reads in total,
so I hope that this could be done pretty soon :-) At least, could you
please check already this week that the files are OK so that I can
modify them if needed without further delay.
Further details in the wiki:
http://www.geuvadis.org/group/geuvadis/wikis/-/wiki/Main%20Geuvadis%20Wiki/…
cheers,
Tuuli
--
Tuuli Lappalainen, PhD
Department of Genetic Medicine and Development
University of Geneva Medical School
CMU / Rue Michel-Servet 1
1211 Geneva 4
Switzerland
Tel. +41-(0)22-3795550
tuuli.lappalainen(a)unige.ch