2016
DOI: 10.3732/apps.1600017
|View full text |Cite
|
Sign up to set email alerts
|

Low‐coverage, whole‐genome sequencing of Artocarpus camansi (Moraceae) for phylogenetic marker development and gene discovery

Abstract: Premise of the study:We used moderately low-coverage (17×) whole-genome sequencing of Artocarpus camansi (Moraceae) to develop genomic resources for Artocarpus and Moraceae.Methods and Results:A de novo assembly of Illumina short reads (251,378,536 pairs, 2 × 100 bp) accounted for 93% of the predicted genome size. Predicted coding regions were used in a three-way orthology search with published genomes of Morus notabilis and Cannabis sativa. Phylogenetic markers for Moraceae were developed from 333 inferred si… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

3
64
0

Year Published

2016
2016
2020
2020

Publication Types

Select...
7

Relationship

5
2

Authors

Journals

citations
Cited by 43 publications
(68 citation statements)
references
References 35 publications
3
64
0
Order By: Relevance
“…S11). A similar pattern of multicopy genes recovered from exon capture data has been reported in Artocarpus (Moraceae; Johnson et al ., ), which is known to have undergone at least one whole genome duplication (Gardner et al ., ). This suggests that the pattern detected in Lachemilla , Alchemilla , and Aphanes might also be the result of an ancient whole genome duplication that predates the diversification of the clade.…”
Section: Discussionmentioning
confidence: 97%
“…S11). A similar pattern of multicopy genes recovered from exon capture data has been reported in Artocarpus (Moraceae; Johnson et al ., ), which is known to have undergone at least one whole genome duplication (Gardner et al ., ). This suggests that the pattern detected in Lachemilla , Alchemilla , and Aphanes might also be the result of an ancient whole genome duplication that predates the diversification of the clade.…”
Section: Discussionmentioning
confidence: 97%
“…Identification of intron‐exon boundaries is possible using MarkerMiner (Chamala et al., ), which aligns transcriptome data to reference genome sequences and returns intron‐masked multiple‐sequence alignments. If no reference genome is available, a low‐coverage genome sequence (10–15× coverage) can also be used to design probes around intron boundaries (Gardner et al., ). Finally, the pipeline Sondovač (Schmickl et al., ) uses a combination of transcriptome and genome skimming data to identify possible nuclear exons, and their introns, to be captured.…”
Section: Target Enrichmentmentioning
confidence: 99%
“…Sequencing libraries were hybridized to a bait set comprising 458 target nuclear coding regions. We describe the development of bait sequences from a draft genome sequence in a companion paper (Gardner et al, 2016). Briefly, 333 loci intended for phylogenetic analysis were selected by identifying long exons homologous between the Artocarpus draft genome and the published genome of Morus notabilis C. K. Schneid.…”
Section: Methods and Resultsmentioning
confidence: 99%
“…A set of 125 additional genes were targeted for their functional significance: 98 MADS-box genes and 27 genes that have been implicated in floral volatiles. For the genes of functional significance, baits were designed from the A. camansi Blanco draft genome alone (Gardner et al, 2016). A set of 20,000 baits (biotinylated RNA oligonucleotides, the smallest MYbaits kit) with 3× tiling was manufactured by MYcroarray (Ann Arbor, Michigan, USA).…”
Section: Methods and Resultsmentioning
confidence: 99%
See 1 more Smart Citation