Кечин Андрей Андреевич

This study identifies large genomic rearrangements and copy number variants in HCT116 cell line samples using Oxford Nanopore sequencing and compares common and unique variants across samples.

eLaRodON improves large genomic rearrangement detection in Oxford Nanopore data, outperforming existing tools with higher accuracy across multiple datasets.

This paper introduces a method combining exome sequencing and chromosome conformation capture to detect both SNVs and SVs, demonstrating its effectiveness in identifying causative variants in rare disorders.

This paper introduces an S1 nuclease-based Hi-C method for chromatin conformation capture, offering improved chromatin fragmentation and library preparation compared to DNase I Hi-C.

The paper analyzes BRCA1 and BRCA2 mutations in ovarian cancer patients from Russia, identifying common and novel variants and estimating the age of a founder mutation.

NGS-PrimerPlex designs primers for multiplex PCR to create NGS panels, achieving high coverage in sequencing the LRRK2 gene.