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Prall, T.

Publications and source records attributed to Prall, T..

2 recordsLinked to original sources

Determinants of haplotype phasing accuracy in long-read human genome sequencing

Accurate haplotype phasing is critical for interpreting human genetic variation. Long-read whole-genome sequencing has emerged as a powerful approach for read-based phasing, particularly where parental DNA is absent, yet the determinants of phasing accuracy remain incompletely defined. Here, we evaluate haplotype phasing performance across sequencing technology, reference genome, read length, and coverage depth using Oxford Nanopore Technologies (ONT) and Pacific Biosciences (PacBio) data from two Genome in a Bottle reference samples (HG002 and HG005). In clinically relevant genes, alignment to the T2T-CHM13 (T2T) reference genome improves phasing performance relative to GRCh38, reducing mean gene-level phasing error rates by 3-9-fold. T2T alignment increases phase set NG50 and yields 1.5-2-fold more phased variant pairs. At similar read N50 values, ONT has a higher phasing error rate than PacBio in certain genes. Downsampling demonstrates that phasing error rates plateau at [~]20x coverage. Longer ONT read lengths reduce phasing error rates and extend phase set contiguity. Haplotype-resolved assemblies produce substantially higher phasing error rates than alignment-based phasing, demonstrating the advantage of an alignment-based approach. To enable per-variant-pair confidence assessment, we introduce PhaseQuality, a technology-specific stratification method that assigns confidence tiers to phased variants based solely on sequencing data. PhaseQuality accurately assigns 82-99% of known phasing errors to lower-confidence tiers, reducing error rates among high-confidence pairs to <0.5%. Together, these results demonstrate the primary technical determinants of long-read haplotype phasing accuracy and provide practical benchmarks for optimizing reference genome selection, coverage targets, and read length for long-read sequencing studies.

genomics↗

Construction of a new chromosome-scale, long-read reference genome assembly of the Syrian hamster, Mesocricetus auratus

BackgroundThe Syrian hamster (Mesocricetus auratus) has been suggested as a useful mammalian model for a variety of diseases and infections, including infection with respiratory viruses such as SARS-CoV-2. The MesAur1.0 genome assembly was generated in 2013 using whole-genome shotgun sequencing with short-read sequence data. Current more advanced sequencing technologies and assembly methods now permit the generation of near-complete genome assemblies with higher quality and greater continuity. FindingsHere, we report an improved assembly of the M. auratus genome (BCM_Maur_2.0) using Oxford Nanopore Technologies long-read sequencing to produce a chromosome-scale assembly. The total length of the new assembly is 2.46 Gbp, similar to the 2.50 Gbp length of a previous assembly of this genome, MesAur1.0. BCM_Maur_2.0 exhibits significantly improved continuity with a scaffold N50 that is 6.7 times greater than MesAur1.0. Furthermore, 21,616 protein coding genes and 10,459 noncoding genes are annotated in BCM_Maur_2.0 compared to 20,495 protein coding genes and 4,168 noncoding genes in MesAur1.0. This new assembly also improves the unresolved regions as measured by nucleotide ambiguities, where approximately 17.11% of bases in MesAur1.0 were unresolved compared to BCM_Maur_2.0 in which the number of unresolved bases is reduced to 3.00%. ConclusionsAccess to a more complete reference genome with improved accuracy and continuity will facilitate more detailed, comprehensive, and meaningful research results for a wide variety of future studies using Syrian hamsters as models.

genomics↗