
Alan Boyle
@ap_boyle
Genomics/Bioinformatics Assoc. Prof., University of Michigan
Msstate, Duke, Stanford, Michigan
Genetic Variation, Silencers, RegulomeDB, Nanopore Tech
ID: 24257253
http://BoyleLab.org 13-03-2009 21:21:38
340 Tweet
478 Followers
704 Following


Really excited to be part of this with Alan Boyle and Mike McConnell! Our part of the project will be focused on exploring somatic mosaicism in single cells as well as targeted capture of specific types of variation in bulk tissue using long read nanopore sequencing.

๐ขNew in Human Genetics and Genomics Advances! Alan Boyle & colleagues explore the challenges posed when screening for de novo variants in complex phenotypes bit.ly/43f86ZE







I am beyond excited to share our new paper on massively parallel reporter assays on schizophrenia-associated variants. This is in collaboration with Jason Stein, Sri Kosuri, Michael Love, Jose Davila Velderrain, Brad Ruzicka, Alan Boyle. ๐งต follows.

Our preprint is out!ย We hacked the Oxford Nanopore sequencer toย read amino acids and PTMs along protein strands. This opens up the possibility for barcode sequencing at the protein level for highly multiplexed assays, PTM monitoring, and protein identification! biorxiv.org/content/10.110โฆ

New Alan Boyle and Todd Lab @UM collaboration is now up on medRxiv ๐ฅณ we used targeted long read sequencing and HMMSTR to successfully identify and genotype known or suspected large tandem repeat expansions at many loci in patient derived samples. medrxiv.org/content/10.110โฆ

Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants hubs.li/Q02v7f3S0 Hyejung Won Jason Stein Sri Kosuri Michael Love @_josedavila Brad Ruzicka Alan Boyle Up-and-coming genomics research from Cell Genomics #neurogenomics

Our first study in a new repeat expansion disorder: CANVAS. Connor Maltby used patient iPSNs to define how this non-reference AAGGG repeat impacts neuronal function. He finds a novel role for the repeat in disease that is independent of RFC1 function science.org/doi/10.1126/scโฆ

Excited to share the white paper for the IGVF Consortium, supported by National Human Genome Research Institute Deciphering the impact of genomic variation on function rdcu.be/dSZdm

New paper from my postdoc work at Michigan Research is now out in Science Advances ๐ very proud to share the culmination of nearly 4 years of hard work with a fantastic group of colleagues and collaborators. A ๐งต of what we found out about RFC1/CANVAS ๐ science.org/doi/10.1126/scโฆ

Our ChromBPNet preprint out! Huge congrats to Anusri Pampari! This was quite a slog for both of us but we r very proud of this one! It is a long read but worth it IMHO. Methods r in the supp. materials. Link in the next tweet. Bluetorial coming soon .. 1/
