Single-nucleus ATAC-seq analysis of lymphangioleiomyomatosis (LAM)

Tasnim F. Olatoke1, Andrew Wagner2, Aristotelis A. Astrinidis1, Francis X. McCormack1, Yan Xu2, Jane J. Yu1
1University of Cincinnati College of Medicine, 2Cincinnati Children's Hospital Medical Center, *Corresponding author
Description Single-nucleus ATAC-seq of lymphangioleiomyomatosis (LAM) lungs to construct gene regulatory network controlling the transcriptional program of LAM cells. In vivo and in vitro LAM models were used to identify molecular mechanisms mediating LAM cell pathogenesis. Integrative single cell omics analyses identified the activation of uterine specific HOX-PBX transcriptional programs in pulmonary LAMCORE cells.
Dataset ID LMEX0000004413
Assay Type Single-nucleus ATAC-seq
Organism Human
Stages Adult | 65+ years
Sample Count 10050
Sample Prep Lmdata:sample_type_single_nucleus
Technology 10x Genomics Chromium Single Cell Multiome ATAC + Gene Expression
External databases GEO: GSE217106
LungMAP IDAlt IDSpeciesSexRaceAgeAge GroupGA at BirthCGAWeightWeight PercentileCause of DeathType of Death
LMSP0000001588D213Homo sapiensFemaleWhite23 monthsChild40 weeks, 3 days143.29 weeks13.7 kg92Lung Disease - Viral PneumoniaDBD (after brain death)
LMSP0000001586LAM3Homo sapiensFemale65 years65+ years
LMSP0000001587LAM32Homo sapiensFemale55 yearsAdult

3 of this study's 3 samples were also assayed by 1 other LungMAP studies, across 1 modality. Click any node to list those studies.