Project description:Phylogenomic inference from low-depth sequencing
| PRJEB29600 | ENA
Project description:Contrasting whole-genome and reduced representation sequencing pipelines for population demographic inference - high coverage genomes
| PRJNA909333 | ENA
Project description:Phylogenomic inference of the higher classification of velvet ants (Hymenoptera: Mutillidae)
| PRJNA912170 | ENA
Project description:Contrasting whole-genome and reduced representation sequencing pipelines for population demographic inference
Project description:In order to validate of CNV detection from low-coverage whole-genome sequencing in the blood samples from recurrent miscarriage couples, we employed a customized array Comparative Genomics Hybridization (aCGH, Agilent) approach as chromosomal microarray analysis (CMA) in present study for a cohort of 78 DNA samples from blood. CMA results were compared with low-coverage whole-genome sequencing detection results. 100% consistency was obtained in pathogenic or likely pathogenic CNVs detection.
