ArticleFrontiers in genetics2020
Genetic Variants Detection Based on Weighted Sparse Group Lasso.
Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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
2 citing papers in PubMed, 7 citations in OpenAlex.
- Article
- Seagull: lasso, group lasso and sparse-group lasso regularization for linear regression models via proximal gradient descent.BMC bioinformatics · 2020Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
5 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Identification of genetic variants associated with complex traits is a critical step for improving plant resistance and breeding. Although the majority of existing methods for variants detection have good predictive performance in the average case, they can not precisely identify the variants present in a small number of target genes. In this paper, we propose a weighted sparse group lasso (WSGL) method to select both common and low-frequency variants in groups. Under the biologically realistic assumption that complex traits are influenced by a few single loci in a small number of genes, our method involves a sparse group lasso approach to simultaneously select associated groups along with the loci within each group. To increase the probability of selecting out low-frequency variants, biological prior information is introduced in the model by re-weighting lasso regularization based on weights calculated from input data. Experimental results from both simulation and real data of single nucleotide polymorphisms (SNPs) associated with
Indexed as
Identifiers
What Socratic holds
Registered trials
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 Socratic graph.