Skip to the content.

in conjunction with IEEE BIBM 2022

Las Vegas, NV, USA

December 6-9, 2022


With the advances of high-throughput DNA and RNA sequencing platforms, sequencing data opens an unprecedented opportunity for genomic variant analysis at genome-wide scale or in single-cell resolution. To date, many algorithms have been designed to detect different types of variants such as single nucleotide polymorphisms (SNPs), small insertions and deletions (indels), and large structural variants (SVs). Wide adoption of these algorithms and tools is expected to facilitate discovery and explicate the genetic causes of complex conditions and cancers.

We invite investigators to contribute Original Research on computational methods of genome reconstruction, detecting and phasing variants. Potential topics include but are not limited to the following:

Important Dates (Tentative)

Program Chairs

Program Committee Members

Workshop Submission Requirement

Please submit a full-length paper (up to 8 page IEEE 2-column format ) through the online submission system (you can download the format instruction here. Electronic submissions (in PDF or Postscript format) are required. Selected participants will be asked to submit their revised papers in a format to be specified at the time of acceptance.

Workshop Online Submission:

Submit a paper Click here


At least one author of an accepted paper needs to register as one full registration in order to have the paper published in the conference proceedings.

Workshop schedule

The workshop will be held on Tuesday, December 7, 2022 (based on USA PST Time), Caesars Palace(Room: Pisa), Las Vegas, USA

time title Presenter/Author
2:00pm-2:20pm High-resolution sample size enrichment of single-cell multi-modal low-throughput Patch-seq datasets Lorenzo Martini, Roberta Bardini, Alessandro Savino, and Stefano Di Carlo
2:20pm-2:40pm Haplotype-phasing of long-read HiFi data to enhance structural variant detection through a Skip-Gram model Can Luo, Parth Datar, Yichen Henry Liu, and Xin Zhou
2:40pm-3:00pm Reliable tumor evolution estimates using bulk sequencing data Jared Huzar, Madelyn Shenoy, Maxwell Sanderford, Sudhir Kumar, and Sayaka Miura
3:00pm-3:20pm Targeted Next generation Sequencing Reveals the Genetic Mechanism of Chinese Marfan syndrome Cohort with Ocular Manifestation Dongming Han, Wei Li, Ziwei Wang, Sicheng Guo, Jiayu Gao, and Jiankang Li