Author

C. Lord

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

Click to filter author papers

Immunology· 3 Cell Biology· 1 Ecology· 1

Signature Assays, Organisms & Methods

Click to filter · or open tag

Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Assay:bulk RNA-seq· 2 Research Focus:cell signaling & trafficking· 2 Approach:deep learning· 2 Research Focus:differential expression· 2 Organism:human· 2 Assay:scRNA-seq· 2

Frequent Co-Authors

A. K. Savage· 3 shared E. Swanson· 3 shared T. R. Torgerson· 3 shared X.-j. Li· 3 shared A. T. Heubeck· 2 shared J. Reading· 2 shared L. T. Graybuck· 2 shared P. J. Skene· 2 shared

Activity by Year

2018-2022 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

3 shared papersImmunology

A. K. Savage

Mutual co-authors in cluster

Author profile →

5 papers

Recent·Most cited

PALMO: a comprehensive platform for analyzing longitudinal multi-omics data

S. V. Vasaikar, A. K. Savage, Q. Gong, E. Swanson, A. Talla, C. Lord, A. Heubeck, J. Reading, L. T. Graybuck, P. Meijer, T. R. Torgerson, P. Skene, T. Bumol, X.-j. Li

PALMO analyzes longitudinal multi-omics data by decomposing variations, identifying stable/variable features, and detecting markers across timepoints, validated on a complex dataset and external benchmarks.

bioRxiv · Oct 17, 2022 · PreprintImmunology

Multimodal Analysis for Human ex vivo Studies Shows Extensive Molecular Changes from Delays in Blood Processing

A. K. Savage, M. V. Gutschow, T. Chiang, K. Henderson, R. Green, M. Chaudhari, E. Swanson, A. T. Heubeck, N. Kondza, K. C. Burley, P. C. Genge, C. Lord, T. Smith, Z. Thomson, A. Beaubien, , T. F. Bumol

This study shows that delayed blood processing causes significant changes in single-cell transcriptomes and plasma proteomes within 6 hours, potentially confounding disease-related biological variance.

bioRxiv · Oct 18, 2020Immunology

TEA-seq: a trimodal assay for integrated single cell measurement of transcription, epitopes, and chromatin accessibility

E. Swanson, C. Lord, J. Reading, A. T. Heubeck, A. K. Savage, R. Green, X.-j. Li, T. R. Torgerson, T. F. Bumol, L. T. Graybuck, P. J. Skene

The paper introduces TEA-seq, a trimodal assay that integrates scRNA-seq, cell surface epitopes, and scATAC-seq to improve single-cell analysis of transcription, epitopes, and chromatin accessibility.

bioRxiv · Sep 4, 2020 · PreprintImmunology

Nuclear envelope-vacuole contacts mitigate nuclear pore complex assembly stress

C. Lord, S. Wente

The paper shows that nuclear envelope-vacuole contacts help yeast cells cope with stress from disrupted NPC assembly, improving viability and NPC formation.

bioRxiv · Mar 23, 2020Cell Biology

Minimum Information for Reusable Arthropod Abundance Data (MIReAAD)

S. S. C. Rund, K. Braak, L. Cator, K. Copas, S. J. Emrich, G. I. Giraldo-Calderon, M. A. Johansson, N. Heydari, D. Hobern, S. A. Kelly, D. Lawson, C. Lord, R. M. MacCallum, D. G. Roche, S. J. Ryan, , S. Pawar

The paper introduces MIReAAD, a framework for standardizing arthropod abundance data to improve reusability and comparability across studies.

bioRxiv · Oct 17, 2018 · PreprintEcology