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Physical separation of haplotypes in dikaryons allows benchmarking of phasing accuracy in Nanopore and HiFi assemblies with Hi-C data
by
Hewitt, Tim
, Figueroa, Melania
, Hu, Yiheng
, Upadhyaya, Narayana M.
, Dodds, Peter N.
, Mago, Rohit
, Stone, Eric A.
, Mackenzie, Amy
, Jones, Ashley W.
, Lewis, David
, Duan, Hongyu
, Rathjen, John P.
, Sperschneider, Jana
, Periyannan, Sambasivam
, Sharp, Anna
, Schwessinger, Benjamin
in
Accuracy
/ Animal Genetics and Genomics
/ Animals
/ Benchmarking
/ Bioinformatics
/ Biomedical and Life Sciences
/ Chromatin
/ Chromosomes
/ Coverage
/ Dikaryons
/ Diploids
/ diploidy
/ Evolutionary Biology
/ Fungi
/ Genome
/ genome assembly
/ Genomes
/ genomics
/ haploidy
/ Haplotypes
/ Heterozygosity
/ Hi-C
/ HiFi
/ High-Throughput Nucleotide Sequencing - methods
/ Human Genetics
/ Infections
/ Leaf rust
/ Life Sciences
/ Long-read sequencing
/ Microbial Genetics and Genomics
/ Nanopores
/ Nuclei
/ Phase switches
/ Phasing
/ Plant Genetics and Genomics
/ Puccinia recondita
/ Sequence Analysis, DNA - methods
/ species
2022
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Physical separation of haplotypes in dikaryons allows benchmarking of phasing accuracy in Nanopore and HiFi assemblies with Hi-C data
by
Hewitt, Tim
, Figueroa, Melania
, Hu, Yiheng
, Upadhyaya, Narayana M.
, Dodds, Peter N.
, Mago, Rohit
, Stone, Eric A.
, Mackenzie, Amy
, Jones, Ashley W.
, Lewis, David
, Duan, Hongyu
, Rathjen, John P.
, Sperschneider, Jana
, Periyannan, Sambasivam
, Sharp, Anna
, Schwessinger, Benjamin
in
Accuracy
/ Animal Genetics and Genomics
/ Animals
/ Benchmarking
/ Bioinformatics
/ Biomedical and Life Sciences
/ Chromatin
/ Chromosomes
/ Coverage
/ Dikaryons
/ Diploids
/ diploidy
/ Evolutionary Biology
/ Fungi
/ Genome
/ genome assembly
/ Genomes
/ genomics
/ haploidy
/ Haplotypes
/ Heterozygosity
/ Hi-C
/ HiFi
/ High-Throughput Nucleotide Sequencing - methods
/ Human Genetics
/ Infections
/ Leaf rust
/ Life Sciences
/ Long-read sequencing
/ Microbial Genetics and Genomics
/ Nanopores
/ Nuclei
/ Phase switches
/ Phasing
/ Plant Genetics and Genomics
/ Puccinia recondita
/ Sequence Analysis, DNA - methods
/ species
2022
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Physical separation of haplotypes in dikaryons allows benchmarking of phasing accuracy in Nanopore and HiFi assemblies with Hi-C data
by
Hewitt, Tim
, Figueroa, Melania
, Hu, Yiheng
, Upadhyaya, Narayana M.
, Dodds, Peter N.
, Mago, Rohit
, Stone, Eric A.
, Mackenzie, Amy
, Jones, Ashley W.
, Lewis, David
, Duan, Hongyu
, Rathjen, John P.
, Sperschneider, Jana
, Periyannan, Sambasivam
, Sharp, Anna
, Schwessinger, Benjamin
in
Accuracy
/ Animal Genetics and Genomics
/ Animals
/ Benchmarking
/ Bioinformatics
/ Biomedical and Life Sciences
/ Chromatin
/ Chromosomes
/ Coverage
/ Dikaryons
/ Diploids
/ diploidy
/ Evolutionary Biology
/ Fungi
/ Genome
/ genome assembly
/ Genomes
/ genomics
/ haploidy
/ Haplotypes
/ Heterozygosity
/ Hi-C
/ HiFi
/ High-Throughput Nucleotide Sequencing - methods
/ Human Genetics
/ Infections
/ Leaf rust
/ Life Sciences
/ Long-read sequencing
/ Microbial Genetics and Genomics
/ Nanopores
/ Nuclei
/ Phase switches
/ Phasing
/ Plant Genetics and Genomics
/ Puccinia recondita
/ Sequence Analysis, DNA - methods
/ species
2022
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Physical separation of haplotypes in dikaryons allows benchmarking of phasing accuracy in Nanopore and HiFi assemblies with Hi-C data
Journal Article
Physical separation of haplotypes in dikaryons allows benchmarking of phasing accuracy in Nanopore and HiFi assemblies with Hi-C data
2022
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Overview
Background
Most animals and plants have more than one set of chromosomes and package these haplotypes into a single nucleus within each cell. In contrast, many fungal species carry multiple haploid nuclei per cell. Rust fungi are such species with two nuclei (karyons) that contain a full set of haploid chromosomes each. The physical separation of haplotypes in dikaryons means that, unlike in diploids, Hi-C chromatin contacts between haplotypes are false-positive signals.
Results
We generate the first chromosome-scale, fully-phased assembly for the dikaryotic leaf rust fungus
Puccinia triticina
and compare Nanopore MinION and PacBio HiFi sequence-based assemblies. We show that false-positive Hi-C contacts between haplotypes are predominantly caused by phase switches rather than by collapsed regions or Hi-C read mis-mappings. We introduce a method for phasing of dikaryotic genomes into the two haplotypes using Hi-C contact graphs, including a phase switch correction step. In the HiFi assembly, relatively few phase switches occur, and these are predominantly located at haplotig boundaries and can be readily corrected. In contrast, phase switches are widespread throughout the Nanopore assembly. We show that haploid genome read coverage of 30–40 times using HiFi sequencing is required for phasing of the leaf rust genome, with 0.7% heterozygosity, and that HiFi sequencing resolves genomic regions with low heterozygosity that are otherwise collapsed in the Nanopore assembly.
Conclusions
This first Hi-C based phasing pipeline for dikaryons and comparison of long-read sequencing technologies will inform future genome assembly and haplotype phasing projects in other non-haploid organisms.
Publisher
BioMed Central,Springer Nature B.V,BMC
Subject
/ Animal Genetics and Genomics
/ Animals
/ Biomedical and Life Sciences
/ Coverage
/ Diploids
/ diploidy
/ Fungi
/ Genome
/ Genomes
/ genomics
/ haploidy
/ Hi-C
/ HiFi
/ High-Throughput Nucleotide Sequencing - methods
/ Microbial Genetics and Genomics
/ Nuclei
/ Phasing
/ Sequence Analysis, DNA - methods
/ species
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