Jonathan Sebat

According to our database, Jonathan Sebat authored at least 5 papers between 2006 and 2021.

Collaborative distances:

• Dijkstra number of four.
• Erdős number of four.

2021

Customized de novo mutation detection for any variant calling pipeline: SynthDNM.

Aojie Lian, James Guevara, Kun Xia, Jonathan Sebat

Bioinform., 2021

2019

Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome.

Kymberleigh A. Pagel, Danny Antaki, Aojie Lian, Matthew E. Mort, David N. Cooper, Jonathan Sebat, Lilia M. Iakoucheva, Sean D. Mooney, Predrag Radivojac

PLoS Comput. Biol., 2019

2018

SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes.

Danny Antaki, William M. Brandler, Jonathan Sebat

Bioinform., 2018

2017

When loss-of-function is loss of function: assessing mutational signatures and impact of loss-of-function genetic variants.

Kymberleigh A. Pagel, Vikas Pejaver, Guan Ning Lin, Hyun-Jun Nam, Matthew E. Mort, David N. Cooper, Jonathan Sebat, Lilia M. Iakoucheva, Sean D. Mooney, Predrag Radivojac

Bioinform., 2017

2006

PROBER: oligonucleotide FISH probe design software.

Nicholas Navin, Vladimir Grubor, Jim Hicks, Evan Leibu, Elizabeth Thomas, Jennifer Troge, Michael Riggs, Pär Lundin, Susanne Månér, Jonathan Sebat, Anders Zetterberg, Michael Wigler

Bioinform., 2006