NGS Services
Molth provides end-to-end next-generation sequencing (NGS) services for discovery, translational research, and biomarker development. From sample prep to bioinformatics, we deliver high-quality libraries, rigorous QC, and actionable results.
What we provide
Customized solutions
Customized evaluation of research projects and identification of the best solutions.
Sample preparation
Tissue and cell sample preparation with rigorous quality control.
NGS data analysis
Development and quality assurance of NGS libraries, followed by deep sequencing and AI-enhanced data analysis.
Service Portfolio
We provide comprehensive NGS services to support academic and translational research:
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Whole-Genome & Whole-Exome Sequencing (WGS/WES): Comprehensive variant and mutation profiling.
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RNA-seq: Transcriptome analysis for expression profiling, fusion detection, and pathway insights.
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ATAC-seq: Chromatin accessibility mapping to reveal regulatory landscapes.
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ChIP-seq: Profiling histone modifications and transcription factor binding.
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CUT&Tag / CUT&RUN: Low-input, high-sensitivity alternatives for epigenomic profiling.
Request more information
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Case studies
Transcriptomic analysis
RNA-seq heatmaps of all deregulated genes in control and RING1B-depleted T47D cells.
Sci Adv. 2020 Jun 5;6(23):eaaz7249.
Chromatic accessibility
PCA on all chromatin peaks from young and old qNSCs and aNSCs.
Nature Aging. 2023 Jul;3(7):866-893.
Histone modifications
Browser tracks show examples of age-dependent changes in histone modifications at promoters and enhancers. Nature Aging. 2024 Jan.