Evidence map›Paper›PMID 28883428›Full record

ArticleScientific reports2017

Assessing SNP genotyping of noninvasively collected wildlife samples using microfluidic arrays.

Alina von Thaden, Berardino Cocchiararo, Anne Jarausch, Hannah Jüngling, Alexandros A Karamanlidis, Annika Tiesmeyer, Carsten Nowak, Violeta Muñoz-Fuentes

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing 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

41 citing papers in PubMed.

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  6. Ecology and evolution · 2026
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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

8 authors.

Alina von ThadenConservation Genetics Group, Senckenberg Research Institute and Natural History Museum Frankfurt, Clamecystraße 12, 63571, Gelnhausen, Germany. alina.vonthaden@senckenberg.de.
Berardino CocchiararoConservation Genetics Group, Senckenberg Research Institute and Natural History Museum Frankfurt, Clamecystraße 12, 63571, Gelnhausen, Germany.
Anne JarauschConservation Genetics Group, Senckenberg Research Institute and Natural History Museum Frankfurt, Clamecystraße 12, 63571, Gelnhausen, Germany.
Hannah JünglingConservation Genetics Group, Senckenberg Research Institute and Natural History Museum Frankfurt, Clamecystraße 12, 63571, Gelnhausen, Germany.
Alexandros A KaramanlidisARCTUROS, Civil Society for the Protection and Management of Wildlife and the Natural Environment, Aetos, GR-53075, Florina, Greece.
Annika TiesmeyerConservation Genetics Group, Senckenberg Research Institute and Natural History Museum Frankfurt, Clamecystraße 12, 63571, Gelnhausen, Germany.
Carsten NowakConservation Genetics Group, Senckenberg Research Institute and Natural History Museum Frankfurt, Clamecystraße 12, 63571, Gelnhausen, Germany. carsten.nowak@senckenberg.de.
Violeta Muñoz-FuentesConservation Genetics Group, Senckenberg Research Institute and Natural History Museum Frankfurt, Clamecystraße 12, 63571, Gelnhausen, Germany. vmunoz@ebi.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Noninvasively collected samples are a common source of DNA in wildlife genetic studies. Currently, single nucleotide polymorphism (SNP) genotyping using microfluidic arrays is emerging as an easy-to-use and cost-effective methodology. Here we assessed the performance of microfluidic SNP arrays in genotyping noninvasive samples from grey wolves, European wildcats and brown bears, and we compared results with traditional microsatellite genotyping. We successfully SNP-genotyped 87%, 80% and 97% of the wolf, cat and bear samples, respectively. Genotype recovery was higher based on SNPs, while both marker types identified the same individuals and provided almost identical estimates of pairwise differentiation. We found that samples for which all SNP loci were scored had no disagreements across the three replicates (except one locus in a wolf sample). Thus, we argue that call rate (amplification success) can be used as a proxy for genotype quality, allowing the reduction of replication effort when call rate is high. Furthermore, we used cycle threshold values of real-time PCR to guide the choice of protocols for SNP amplification. Finally, we provide general guidelines for successful SNP genotyping of degraded DNA using microfluidic technology.

Indexed as

Polymorphism, Single NucleotideAnimalsAnimals, WildCatsFecesGenotyping TechniquesHairMicrofluidicsUrsidaeWolves

Identifiers

PMID28883428
PMCPMC5589735

What OpenQuestion holds

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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.