Identifying rare variants from exome scans: the GAW17 experience.

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.

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.

Who cites it

3 citing papers in PubMed.

1. Detecting the Genomic Signature of Divergent Selection in Presence of Gene Flow.Current genomics · 2015
   Article
2. Rare variants detection with kernel machine learning based on likelihood ratio test.PloS one · 2014
   Article
3. The role of phenotype in gene discovery in the whole genome sequencing era.Human genetics · 2012
   Review

Corrections and comments

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

Authors and funding

25 authors.

Funding

Abstract