Chase Miller

Biologist, Computer Scientist, CoFounder Frameshift Genomics

[Alistair Ward @AlistairNWard]

We've added a lot of new functionality to Mosaic. See the tutorial for more details: https://t.co/3OeTWmrxd7

[Erik Garrison @erikgarrison]

#SARSCoV2 pangenome made from 50 genomes in genbank. Top, graph viz and detail showing SNP bubbles. Middle: matrix view of genomes versus nodes in the graph. Bottom: genes versus the pangenome. CC @jervenbolleman @simonheumos @JosiahSeaman

[Chase Miller @ChaseAllnMiller]

How we can offer free, unlimited genomic samples in Mosiac (w/o going bankrupt!) https://t.co/9GtvH20aqC

[Chase Miller @ChaseAllnMiller]

Deeply Integrating Visualization in Genomics. https://t.co/PgkaCKm8QF. A new blog post with some ideas on how to better utilize visualization throughout a genomics workflow instead of just at the end.

[Chase Miller @ChaseAllnMiller]

@zevkronenberg @4urelie Haven't tested that yet, but I would think it would be just fine. Do you know of a long-read public dataset that's on S3? We can give it a try.

[Chase Miller @ChaseAllnMiller]

Excited to release a free version of our genomic visualization & analytics platform, Mosaic. Add unlimited samples (AWS S3 so far). Organize projects across buckets, add teammates, & better understand your data. https://t.co/BlUaWr38AS . Overview Video https://t.co/LrYUlUwY6B

[Chase Miller @ChaseAllnMiller]

@bioigor Here's a screenshot. Also, there are example projects ready to play with as soon as you create an account.

[Gabor Marth @MarthGabor]

A brand new https://t.co/NpfgJoYquZ app just out! https://t.co/IpJUE8DSYk helps you create a list of candidate genes corresponding to the patient's disease and phenotype, using commercially available panel tests. Details at: https://t.co/Mi4lxP82F6 .

[Gabor Marth @MarthGabor]

gene.iobio v3.0 is out! Simple, clean new look, REVEL scores, variant prioritization across list of candidate genes: https://t.co/eOlJ36GJNd

[Chase Miller @ChaseAllnMiller]

The iobio team just released a new version of gene.iobio with gnomAD allele frequency support and some extra ClinVar features. Read more about it on the blog post https://t.co/O5ZCpJjlOU

[Gabor Marth @MarthGabor]

Towards genomic patient analysis at the point of care: https://t.co/OLunmpSfu4

[Alistair Ward @AlistairNWard]

Got confirmation of @frameshift_labs 3rd small business grant late last night. @NIH are burning the midnight oil!

[Alistair Ward @AlistairNWard]

Just received funding confirmation for our second @NIH small business grant at @frameshift_labs. Onwards and upwards...

[Alistair Ward @AlistairNWard]

gene.iobio now allows exporting of data. Another big step forwards! https://t.co/JieKCmiMl9

[Alistair Ward @AlistairNWard]

gene.iobio has had a big upgrade. New interface and lots of new functionality. This post gives a brief summary.
https://t.co/Fb8xKOtCPR

[HangryCrate @hangrycrate]

Thanks to our first customers, we just gave 110 meals to @FeedingAmerica!

[Alistair Ward @AlistairNWard]

gene.iobio now supports the GRCh38 human reference genome (https://t.co/sBjU6pgv4C). Contact the iobio team if interested in other genomes

[Alistair Ward @AlistairNWard]

Just included a quick blog post on how to visualize ClinVar variants with #iobio. @NCBI_Clinical

[Chase Miller @ChaseAllnMiller]

@bjoerngruening @galaxyproject No worries. Thanks for all the hard work you put into it!

[Chase Miller @ChaseAllnMiller]

@martenson Thanks for the heads up. It's been updated! Really like the new logos