The Lithuanian reference genome LT1 - a human de novo genome assembly with short and long read sequence and Hi-C data
Preprint
Abstract
We present LT1, the first high-quality human reference genome from the Baltic States. LT1 is a female de novo human reference genome assembly constructed using 57× of ultra-long nanopore reads and 47× of short paired-end reads. We also utilized 72 Gb of Hi-C chromosomal mapping data to maximize the assembly’s contiguity and accuracy. LT1’s contig assembly was 2.73 Gbp in length comprising of 4,490 contigs with an N50 value of 13.4 Mbp. After scaffolding with Hi-C data and extensive manual curation, we produced a chromosome-scale assembly with an N50 value of 138 Mbp and 4,699 scaffolds. Our gene prediction quality assessment using BUSCO identify 89.3% of the single-copy orthologous genes included in the benchmarking set. Detailed characterization of LT1 suggested it has 73,744 predicted transcripts, 4.2 million autosomal SNPs, 974,000 short indels, and 12,330 large structural variants. These data are shared as a public resource without any restrictions and can be used as a benchmark for further in-depth genomic analyses of the Baltic populations.Keywords
This publication has 47 references indexed in Scilit:
- A new era of long-read sequencing for cancer genomicsJournal of Human Genetics, 2019
- Tools and Strategies for Long-Read Sequencing and De Novo Assembly of Plant GenomesTrends in Plant Science, 2019
- BUSCO: Assessing Genome Assembly and Annotation Completeness2019
- Whole-Genome Annotation with BRAKER2019
- Analysis of pathogenic variants from the ClinVar database in healthy people using next-generation sequencingGenetics Research, 2017
- Juicer Provides a One-Click System for Analyzing Loop-Resolution Hi-C ExperimentsCell Systems, 2016
- A population‐based single nucleotide polymorphism array analysis of genomic aberrations in younger adult acute lymphoblastic leukemia patientsGenes, Chromosomes and Cancer, 2015
- Assessing Rare Variation in Complex Traits2015
- Ancient human genomes suggest three ancestral populations for present-day EuropeansNature, 2014
- A novel de novo 2.5 Mb microdeletion of 7q22.1 harbours candidate gene for neurobehavioural disorders and mental retardationJournal of Genetics, 2014