Bioinformatics Services

All Bioinformatics Core analyses start with standard quality control reporting of the raw sequenced reads. Depending on the assay performed, we offer a wide variety of standardized pipelines (see below). We are also available for consulting before, during, and after project completion to assist in everything from experimental design and planning, to bespoke visualizations, and assistance with uploading of sequence data and results to NCBI GEO for publication. 

Available Pipelines

Analysis

Services

Whole Genome / Exome (WGS/WES) Sequencing 

  • Quality control of fastq files
  • Variant calling (SNVs/INDELs)
  • Copy number (CN) analysis
Bulk RNA-seq
  • Quality control of fastq files
  • Quality control of sequencing libraries
    • RLE boxplots, Library density plots, Sample-vs-sample correlations, MA-plots
  • Dimensionality reduction and visualization
    • Principal components analysis (PCA) and unsupervised clustering (heatmap)
  • Differential expression (DE) analysis
    • Volcano and MA plot output for each experimental contrast
    • Results spreadsheet
  • Gene set testing
  • Over-representation analysis (Gene ontology)
ChIP-seq / CUT&RUN
  • Quality control of fastq files
  • Quality control of sequencing libraries
  • Peak calling / sliding window analysis
    • Peak annotation
    • Bigwig files of peaks for track browser visualization
  • Differential Abundance (DA) testing
    • Volcano and MA plot output for each experimental contrast
  • Motif analysis
Bulk ATAC-seq
  • Quality control of fastq files
  • Quality control of sequencing libraries
    • Fragment size distribution, library complexity, PT ratio, TSS enrichment
  • Peak calling / sliding window analysis
    • Peak annotation
    • Bigwig files for track browser visualization
  • Dimensionality reduction and visualization
  • Differential Abundance (DA) testing
    • Volcano and MA plot output for each experimental contrast
  • Motif analysis
PRO-seq
  • Quality control of fastq files
  • Quality control of sequencing libraries
  • Bigwig files of enrichment for track browser visualization
    • TSS enrichment profiles and heatmaps
  • Promoter-proximal pause index calculation
  • Dimensionality reduction and visualization
  • Differential Pausing
Reduced representation bisulfite sequencing (RRBS)
  • Quality control of raw fastq files
  • Quality control of sequencing library composition
  • Dimensionality reduction and visualization
  • Differential methylation analysis
  • Gene set testing
  • Over-representation testing (Gene ontology)
Single-cell RNA-seq
  • Quality control of raw fastq files
  • Quality control of sequencing library composition
  • Dimensionality reduction and visualization
    • UMAP / tSNE
  • Clustering analysis
  • Cell type prediction
  • Differential expression analysis
    • Cluster-level or pseudobulk
  • Gene set testing
  • Over-representation testing (Gene ontology)
Single-cell multiome
  • Quality control of raw fastq files
  • Quality control of sequencing library composition
  • Dimensionality reduction and visualization
    • UMAP / tSNE
  • Clustering analysis
  • Cell type prediction
  • Differential expression analysis
    • Cluster-level or pseudobulk
  • Differential abundance analysis
  • Feature linkage
  • Gene set testing
  • Over-representation testing (Gene ontology)

Fees

Estimated cost per sample for bulk type analysis:

Samples Hours Price
6 4 $1,000
9 6 $1,500
12 8 $2,000
15 10 $2,500
25 12 $3,000
>25 Contact for quote

Estimated cost per single-cell type analysis:

Samples Hours Price
6 8 $2,000
9 10 $2,500
12 12 $3,000
15 14 $3,500
25 16 $4,000
>25 Contact for quote

Estimated cost also includes a one-hour meeting with the bioinformatics team member(s) to review results. Any additional analysis outside this scope of work will be billed hourly.