Edmund Miller
@edmundmiller.dev
1.4K followers
1.9K following
70 posts
PhD Candidate @ UT Dallas in the Functional Genomics Lab working on Nascent RNA identification
@nf-co.re
Bioinformatics Engineer @seqera.io
https://link.edmundmiller.dev/
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Reposted by Edmund Miller
Yo Akiyama
@yoakiyama.bsky.social
· Aug 5
Scaling down protein language modeling with MSA Pairformer
Recent efforts in protein language modeling have focused on scaling single-sequence models and their training data, requiring vast compute resources that limit accessibility. Although models that use ...
biorxiv.org
Reposted by Edmund Miller
Reposted by Edmund Miller
Pooja Kathail
@poojakathail.bsky.social
· Nov 20
Leveraging genomic deep learning models for non-coding variant effect prediction
The majority of genetic variants identified in genome-wide association studies of complex traits are non-coding, and characterizing their function remains an important challenge in human genetics. Gen...
arxiv.org
Reposted by Edmund Miller
Reposted by Edmund Miller
Seqera
@seqera.io
· Jun 24
Powering Interactive Omics Analysis with BigOmics Analytics and Studios | Seqera
Join us for an insightful webinar with BigOmics Analytics as we showcase the integration of Omics Playground into Studios as a powerful new way to interactively explore RNA-Seq and proteomics results ...
hubs.la
Reposted by Edmund Miller
Reposted by Edmund Miller
Reposted by Edmund Miller
Reposted by Edmund Miller
Reposted by Edmund Miller
Seqera
@seqera.io
· May 6
Scaling the Future of Scientific Software: Seqera Raises $26M Series B
Today, we're ecstatic to announce that Seqera has raised $26 million in Series B funding, led by Addition with participation from Speedinvest, Talis, Amino Collective, BoxOne, and SNR. This milestone ...
hubs.la
Reposted by Edmund Miller
Edmund Miller
@edmundmiller.dev
· Mar 26
Reposted by Edmund Miller
Reposted by Edmund Miller
Edmund Miller
@edmundmiller.dev
· Jan 29
Reposted by Edmund Miller