Evidence map›Paper›PMID 26039588›Full record

ArticleScientific reports2015

Illumina Synthetic Long Read Sequencing Allows Recovery of Missing Sequences even in the "Finished" C. elegans Genome.

Runsheng Li, Chia-Ling Hsieh, Amanda Young, Zhihong Zhang, Xiaoliang Ren, Zhongying Zhao

Abstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

33 citing papers in PubMed.

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  13. Review
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  18. Recompleting theGenome research · 2019
    Article
  19. Technological advances in maize breeding: past, present and future.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2019
    Review
  20. Article
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

6 authors.

Runsheng LiDepartment of Biology, Hong Kong Baptist University, 224 Waterloo Road, Kowloon Tong, Hong Kong, China.
Chia-Ling HsiehIllumina Inc., 5200 Illumina Way, San Diego, 92122, USA.
Amanda YoungIllumina Inc., 5200 Illumina Way, San Diego, 92122, USA.
Zhihong ZhangIllumina Inc., 5200 Illumina Way, San Diego, 92122, USA.
Xiaoliang RenDepartment of Biology, Hong Kong Baptist University, 224 Waterloo Road, Kowloon Tong, Hong Kong, China.
Zhongying Zhao1] Department of Biology, Hong Kong Baptist University, 224 Waterloo Road, Kowloon Tong, Hong Kong, China [2] State Key Laboratory of Environmental and Biological Analysis, Hong Kong Baptist University, Hong Kong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Most next-generation sequencing platforms permit acquisition of high-throughput DNA sequences, but the relatively short read length limits their use in genome assembly or finishing. Illumina has recently released a technology called Synthetic Long-Read Sequencing that can produce reads of unusual length, i.e., predominately around 10 Kb. However, a systematic assessment of their use in genome finishing and assembly is still lacking. We evaluate the promise and deficiency of the long reads in these aspects using isogenic C. elegans genome with no gap. First, the reads are highly accurate and capable of recovering most types of repetitive sequences. However, the presence of tandem repetitive sequences prevents pre-assembly of long reads in the relevant genomic region. Second, the reads are able to reliably detect missing but not extra sequences in the C. elegans genome. Third, the reads of smaller size are more capable of recovering repetitive sequences than those of bigger size. Fourth, at least 40 Kbp missing genomic sequences are recovered in the C. elegans genome using the long reads. Finally, an N50 contig size of at least 86 Kbp can be achieved with 24 × reads but with substantial mis-assembly errors, highlighting a need for novel assembly algorithm for the long reads.

Indexed as

GenomeHigh-Throughput Nucleotide SequencingAnimalsCaenorhabditis elegansGenetic VariationINDEL MutationMolecular Sequence DataRepetitive Sequences, Nucleic AcidReproducibility of Results

Identifiers

PMID26039588
PMCPMC4650653

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Registered trials

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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.