Evidence map›Paper›PMID 27278669›Full record

ArticleScientific reports2016

Genomic leftovers: identifying novel microsatellites, over-represented motifs and functional elements in the human genome.

Natalie C Fonville, Karthik Raja Velmurugan, Hongseok Tae, Zalman Vaksman, Lauren J McIver, Harold R Garner

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
3.4field-weighted citation impact, top 8% of its field
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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

6 authors at 1 institution in 1 country.

Natalie C FonvilleVia Bioinformatics and Clinical Genetics Network, Edward Via College of Osteopathic Medicine, 2265 Kraft Dr, Blacksburg, VA 24060, USA.
Karthik Raja VelmuruganVia Bioinformatics and Clinical Genetics Network, Edward Via College of Osteopathic Medicine, 2265 Kraft Dr, Blacksburg, VA 24060, USA.
Hongseok TaeVia Bioinformatics and Clinical Genetics Network, Edward Via College of Osteopathic Medicine, 2265 Kraft Dr, Blacksburg, VA 24060, USA.
Zalman VaksmanVia Bioinformatics and Clinical Genetics Network, Edward Via College of Osteopathic Medicine, 2265 Kraft Dr, Blacksburg, VA 24060, USA.
Lauren J McIverVia Bioinformatics and Clinical Genetics Network, Edward Via College of Osteopathic Medicine, 2265 Kraft Dr, Blacksburg, VA 24060, USA.
Harold R GarnerVia Bioinformatics and Clinical Genetics Network, Edward Via College of Osteopathic Medicine, 2265 Kraft Dr, Blacksburg, VA 24060, USA.
Edward Via College of Osteopathic Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human genome is 99% complete. This study contributes to filling the 1% gap by enriching previously unknown repeat regions called microsatellites (MST). We devised a Global MST Enrichment (GME) kit to enrich and nextgen sequence 2 colorectal cell lines and 16 normal human samples to illustrate its utility in identifying contigs from reads that do not map to the genome reference. The analysis of these samples yielded 790 novel extra-referential concordant contigs that are observed in more than one sample. We searched for evidence of functional elements in the concordant contigs in two ways: (1) BLAST-ing each contig against normal RNA-Seq samples, (2) Checking for predicted functional elements using GlimmerHMM. Of the 790 concordant contigs, 37 had an exact match to at least one RNA-Seq read; 15 aligned to more than 100 RNA-Seq reads. Of the 249 concordant contigs predicted by GlimmerHMM to have functional elements, 6 had at least one exact RNA-Seq match. BLAST-ing these novel contigs against all publically available sequences confirmed that they were found in human and chimpanzee BAC and FOSMID clones sequenced as part of the original human genome project. These extra-referential contigs predominantly contained pentameric repeats, especially two motifs: AATGG and GTGGA.

Indexed as

Microsatellite RepeatsAlgorithmsAnimalsCell LineContig MappingGenome, HumanGenomicsHumansPan troglodytesSequence Analysis, DNASequence Analysis, RNA

Identifiers

PMID27278669
PMCPMC4899811
OpenAlexW2417419445

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.