Peter Robinson
@pnrobins
Followers
205
Following
2K
Statuses
434
Dear everybody, I have followed the developments in Twitter over the last year with no small disappointment, and have decided that I do not want to continue to be part of a platform that is doing so little to prevent racist and fascist messages from being distributed. Goodbye
0
0
1
RT @hp_ontology: HPO goes international in our new publication «The Human Phenotype Ontology in 2024: phenotypes around the world» https:/…
0
13
0
With our food systems on the verge of collapse, it’s the plutocrats v life on Earth | George Monbiot
0
1
0
RT @PhillipCompeau: This is the best video to introduce a computational biology course. There will never be a better one
0
632
0
Proud to be a part of this effort!
Big announcement today. @hp_ontology goes multi-lingual: Thanks to all translators, @NicoMatentzoglu, and @pnrobins
@MonarchInit
0
0
5
Alternative splicing is coupled to gene expression in a subset of variably expressed genes
0
1
3
I am deeply honored and delighted to be awarded a Humboldt Professorship for AI:
10
6
64
Cool work from the Hunter lab!
Our ignorance-base paper is out! Knowledge is important, but the biomedical literature is also full of open questions, controversies, and other statements regarding scientific ignorance. Text-mining for them has interesting applications...
0
0
2
RT @Tiff_callahan: We did it!! 💪🥳 This work was started during my PhD @CUAnschutz and completed during my Postdoctoral Fellowship @Columbia…
0
10
0
RT @GHGA_DE: We are excited to welcome Peter Robinson (@pnrobins) from the @jacksonlab to #GHGAtalks today! He is talking about "The Phen…
0
2
0
RT @jacksonlab: 📙 New in Bioinformatics from @OUPAcademic: "An expectation-maximization framework for comprehensive prediction of isoform-s…
0
2
0
RT @drseb_: Big announcement today. @hp_ontology goes multi-lingual: Thanks to all translators, @NicoMatentzoglu,…
0
10
0
Individualised human phenotype ontology gene panels improve clinical whole exome and genome sequencing analytical efficacy in a cohort of developmental and epileptic encephalopathies
1
1
4