Evidence map›Paper›PMID 40779103›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Building Portable and Reproducible Cancer Informatics Workflows for Scalable Data Analysis: An RNA Sequencing Tutorial.

Rowan F Beck, Zelia F Worman, Gaurav Kaushik, Brandi N Davis-Dusenbery

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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.

2 · The registry

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.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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

5 · Who and what money

Authors and funding

4 authors.

Rowan F BeckVelsera, Charlestown, MA, USA.
Zelia F WormanVelsera, Charlestown, MA, USA.
Gaurav KaushikScienceIO, New York, NY, USA.
Brandi N Davis-DusenberyIndependent Advisor, Charlestown, MA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The continued decrease in sequencing costs has led to an abundance of high-throughput data representing an increasing diversity of experimental conditions. These changes have been coupled with the adoption of cloud technologies and interoperability standards to share and analyze large primary and secondary data files. While 10 years ago analysis of hundreds or thousands of genomics samples was only practical at institutions with large local computational resources, these experiments can now be routinely performed by anyone with access to the Internet.In this tutorial, we use the Seven Bridges Cancer Genomics Cloud (CGC) to analyze RNA sequencing data from the NIH Cancer Research Data Commons (CRDC). This tutorial demonstrates how to bring a new computational algorithm to the platform, combine it with an existing workflow, and execute an analysis on the cloud. We highlight best practices for designing command line tools, Docker containers, and CWL descriptions to enable massively parallelized and reproducible biomedical computation with cloud resources. The CGC's support for diverse analysis techniques and user-friendly interface simplifies the complex process of handling large datasets while promoting collaboration across disciplines.

Indexed as

Computational BiologyNeoplasmsSequence Analysis, RNAAlgorithmsCloud ComputingData AnalysisGenomicsHigh-Throughput Nucleotide SequencingHumansSoftwareWorkflowAWSBioinformaticsCancer informaticsCloudCWLDockerReproducibilitySoftware designTCGAWorkflows

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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 OpenQuestion graph.