scispace - formally typeset
Open AccessJournal ArticleDOI

The impact of third generation genomic technologies on plant genome assembly.

Reads0
Chats0
TLDR
Since the introduction of next generation sequencing, plant genome assembly projects do not need to rely on dedicated research facilities or community-wide consortia anymore, even individual research groups can sequence and assemble the genomes they are interested in.
About
This article is published in Current Opinion in Plant Biology.The article was published on 2017-04-01 and is currently open access. It has received 170 citations till now. The article focuses on the topics: Hybrid genome assembly & Sequence assembly.

read more

Citations
More filters
Journal ArticleDOI

RIdeogram: drawing SVG graphics to visualize and map genome-wide data on the idiograms.

TL;DR: The visualization of genome-wide data mapping and comparison allow users to quickly establish a clear impression of the chromosomal distribution pattern, thus making RIdeogram a useful tool for any researchers working with omics.
Journal ArticleDOI

SyRI: finding genomic rearrangements and local sequence differences from whole-genome assemblies.

TL;DR: SyRI is presented, a pairwise whole-genome comparison tool for chromosome-level assemblies that starts by finding rearranged regions and then searches for differences in the sequences, which are distinguished for residing in syntenic or rearrange regions.
Journal ArticleDOI

Plant Phenotyping: Past, Present, and Future

TL;DR: The technological advancement that laid the foundation for the development of phenotyping centers is sketched and the upcoming challenges for further advancement of plant phenotypes specifically with respect to standardization of data acquisition and reusability are evaluated.
References
More filters
Journal ArticleDOI

Haplotype-resolved whole-genome sequencing by contiguity-preserving transposition and combinatorial indexing

TL;DR: An approach for genome-wide haplotyping based on contiguity-preserving transposition (CPT-seq) and combinatorial indexing that could enable haplotype resolution to become routine in human genome sequencing.
Journal ArticleDOI

Illumina TruSeq synthetic long-reads empower de novo assembly and resolve complex, highly-repetitive transposable elements

TL;DR: A novel Illumina technology called TruSeq synthetic long-reads is applied, which enables placement of individual TE copies in their proper genomic locations as well as accurate reconstruction of TE sequences, and offers a powerful approach to improve de novo assemblies of whole genomes.
Posted ContentDOI

Phased Diploid Genome Assembly with Single Molecule Real-Time Sequencing

TL;DR: The FALCON-based assemblies were substantially more contiguous and complete than alternate short or long-read approaches, and enabled the study of haplotype structures and heterozygosities between the homologous chromosomes, including identifying widespread heterozygous structural variations within the coding sequences.
Related Papers (5)