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Comparison of C. elegans and C. briggsae Genome Sequences Reveals Extensive Conservation of Chromosome Organization and Synteny

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TLDR
The conservation of both chromosomal organization and synteny between these two distantly related species suggests roles for chromosome organization in the fitness of an organism that is only poorly understood presently.
Abstract
To determine whether the distinctive features of Caenorhabditis elegans chromosomal organization are shared with the C briggsae genome, we constructed a single nucleotide polymorphism–based genetic map to order and orient the whole genome shotgun assembly along the six C briggsae chromosomes Although these species are of the same genus, their most recent common ancestor existed 80–110 million years ago, and thus they are more evolutionarily distant than, for example, human and mouse We found that, like C elegans chromosomes, C briggsae chromosomes exhibit high levels of recombination on the arms along with higher repeat density, a higher fraction of intronic sequence, and a lower fraction of exonic sequence compared with chromosome centers Despite extensive intrachromosomal rearrangements, 1:1 orthologs tend to remain in the same region of the chromosome, and colinear blocks of orthologs tend to be longer in chromosome centers compared with arms More strikingly, the two species show an almost complete conservation of synteny, with 1:1 orthologs present on a single chromosome in one species also found on a single chromosome in the other The conservation of both chromosomal organization and synteny between these two distantly related species suggests roles for chromosome organization in the fitness of an organism that are only poorly understood presently

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Journal ArticleDOI

Genomic signatures of selection at linked sites: unifying the disparity among species

TL;DR: The dominant features that could drive differences in linked selection among species are characterized — including roles for selective sweeps being 'hard' or 'soft' — and the concealing effects of demography and confounding genomic variables are characterized.
Book

Sex Chromosomes and Sex-Linked Genes

乾 大野
TL;DR: Evidence is provided that the X and the Y or the Z and the W were Originally an Homologous Pair of Ordinary Chromosomes, and the Conservation of the Original X or Z.
Journal ArticleDOI

Dispersal and gene flow in free-living marine nematodes

TL;DR: In this paper, the importance of priority effects, founder effects and genetic bottlenecks for population structuring between patches <1 km apart is discussed. And the authors discuss the presence of substantial cryptic diversity in marine nematodes, and end with highlighting future important steps to further unravel nematode evolution and diversity.
Journal ArticleDOI

Holocentric chromosomes: convergent evolution, meiotic adaptations, and genomic analysis

TL;DR: This review describes how holocentricity may be identified through cytological and molecular methods and how extensive genome sequencing and experiments in nonmodel organisms may allow Holocentric chromosomes to shed light on general principles of chromosome segregation.
Journal ArticleDOI

Divergence Times in Caenorhabditis and Drosophila Inferred from Direct Estimates of the Neutral Mutation Rate

TL;DR: Divergence times are inferred among 6 species each of Caenorhabditis and Drosophila, based on thousands of orthologous groups of genes, and direct estimates of the mutation rate from contemporary populations that are corrected for interfering effects of selection are illustrated.
References
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Book ChapterDOI

Primer3 on the WWW for general users and for biologist programmers.

TL;DR: This chapter assumes acquaintance with the principles and practice of PCR, as outlined in, for example, refs.
Journal ArticleDOI

Base-calling of automated sequencer traces using Phred. I. accuracy assessment

TL;DR: In this article, a base-calling program for automated sequencer traces, phred, with improved accuracy was proposed. But it was not shown to achieve a lower error rate than the ABI software, averaging 40%-50% fewer errors in the data sets examined independent of position in read, machine running conditions, or sequencing chemistry.
Journal ArticleDOI

Initial sequencing and comparative analysis of the mouse genome.

Robert H. Waterston, +222 more
- 05 Dec 2002 - 
TL;DR: The results of an international collaboration to produce a high-quality draft sequence of the mouse genome are reported and an initial comparative analysis of the Mouse and human genomes is presented, describing some of the insights that can be gleaned from the two sequences.
Journal ArticleDOI

Base-Calling of Automated Sequencer Traces Using Phred. II. Error Probabilities

TL;DR: The ability to estimate a probability of error for each base-call, as a function of certain parameters computed from the trace data, is developed and implemented in the base-calling program.
Journal ArticleDOI

Finishing the euchromatic sequence of the human genome

Chris P. Ponting, +1 more
- 21 Oct 2004 - 
TL;DR: The current human genome sequence (Build 35) as discussed by the authors contains 2.85 billion nucleotides interrupted by only 341 gaps and is accurate to an error rate of approximately 1 event per 100,000 bases.
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