Evidence map›Paper›PMID 24552708›Full record

ArticleMolecules and cells2014

Genome-wide SNP calling using next generation sequencing data in tomato.

Ji-Eun Kim, Sang-Keun Oh, Jeong-Hee Lee, Bo-Mi Lee, Sung-Hwan Jo

Abstract read
In one paragraph

Article in Molecules and cells, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed.

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  11. Age-Dependent Growth-Related QTL Variations in Pacific Abalone,International journal of molecular sciences · 2023
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  14. Population Genetic Analysis in Persimmons (Plants (Basel, Switzerland) · 2023
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Ji-Eun KimSEEDERS Inc., Daejeon 305-509, Korea.
Sang-Keun Oh
Jeong-Hee Lee
Bo-Mi Lee
Sung-Hwan Jo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The tomato (Solanum lycopersicum L.) is a model plant for genome research in Solanaceae, as well as for studying crop breeding. Genome-wide single nucleotide polymorphisms (SNPs) are a valuable resource in genetic research and breeding. However, to do discovery of genome-wide SNPs, most methods require expensive high-depth sequencing. Here, we describe a method for SNP calling using a modified version of SAMtools that improved its sensitivity. We analyzed 90 Gb of raw sequence data from next-generation sequencing of two resequencing and seven transcriptome data sets from several tomato accessions. Our study identified 4,812,432 non-redundant SNPs. Moreover, the workflow of SNP calling was improved by aligning the reference genome with its own raw data. Using this approach, 131,785 SNPs were discovered from transcriptome data of seven accessions. In addition, 4,680,647 SNPs were identified from the genome of S. pimpinellifolium, which are 60 times more than 71,637 of the PI212816 transcriptome. SNP distribution was compared between the whole genome and transcriptome of S. pimpinellifolium. Moreover, we surveyed the location of SNPs within genic and intergenic regions. Our results indicated that the sufficient genome-wide SNP markers and very sensitive SNP calling method allow for application of marker assisted breeding and genome-wide association studies.

Indexed as

Polymorphism, Single NucleotideGenome, PlantGenome-Wide Association StudyHigh-Throughput Nucleotide SequencingPlant ProteinsSequence Analysis, DNASolanum lycopersicumTranscriptomePlant Proteins

Identifiers

PMID24552708
PMCPMC3907006

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.