Services

RNA Sequencing

  • Study design: Samples, Library prep protocol, Sequencing depth, Sequencing provider.
  • Quality Control: QC of the raw FASTQ data
  • Sequence Alignment: BAM file, Data Summarization, IGV Visualization
  • Expression Quantification: FPKM, TPM, Sample Correlations.     
  • Differential expression analysis: Up-regulated and down-regulated genes.
  • Gene ontology and pathway analysis: Enriched gene ontology and pathways.
  • De novo transcriptome assembly: de novo mRNA assemblies.
  • Novel mRNA, microRNA, lncRNA, circRNA, tsRNA: Novel transcript identifications by comparing with ENSEMBLE/RefSeq gene annotations. 

DNA Sequencing

  • WES, WGS, or Target Enrichment Sequencing
  • Study design: Samples, Library prep protocol, Sequencing depth, Sequencing provider
  • Quality Control: QC of the raw FASTQ data
  • Sequence Alignment: BAM file, Data Summarization, IGV Visualization
  • On target and off-target: on-target rate, Uniformity, Duplication reads     
  • Variant calling: SNPs and INDELs calling
  • Variant calling and annotations: Annovar, ClinVar, OMIM, etc. 
  • Somatic mutations
  • Copy Number Variations

Epigenetics Sequencing

  • Bisulfite Sequencing: WGBS, RRBS, oxBS
  • Study design: Samples, Library prep protocol, Sequencing depth, Sequencing provider
  • Quality Control: QC of the raw FASTQ data
  • Sequence Alignment: BAM file, Data Summarization.
  • Methylation analysis: C to T convertion rate,  methylation for CpG, CHG, CHH. 

ATAC-Seq

  • Study design: Samples, Library prep protocol, Sequencing depth, Sequencing provider.
  • Quality Control: QC of the raw FASTQ data
  • Sequence Alignment: BAM file, Data Summarization, IGV Visualization.
  • Duplicate reads.Insert size of the library. 
  • chrM reads. 
  • TSS score and Blacklist peaks, 
  • Peaking calling: chromatin structure.
  • Peak annotations and interpretations. 

Ribosome profiling

  • Ribo-Seq and RNA-Seq 
  • Study design: Samples, Library prep protocol, Sequencing depth, Sequencing provider.
  • Quality Control: QC of the raw FASTQ data
  • Sequence Alignment: BAM file, Data Summarization, IGV Visualization.
  • Ribosome protected fragments. 
  • Three-nucleotide periodicity. 
  • Translation Efficiency for each gene. 
  • Differentially Translation Efficiency changed gene analysis.

Single Cell Sequencing

  • Single Cell RNA-Seq and Single Cell ATAC-Seq
  • Study design: Samples, Library prep protocol, Sequencing depth, Sequencing provider.
  • Quality Control: QC of the raw FASTQ data
  • Sequence Alignment: BAM file, Data Summarization, IGV Visualization.
  • Duplicate reads. 
  • Number of cells. 
  • Number of genes.
  • Raw read counts and clustering analysis.
  • Peak calling from ATAC-Seq 

Long Read Sequencing

  • PacBio Sequencing and Nanopore Sequencing
  • Study design: Samples, Library prep protocol, Sequencing depth, Sequencing provider.
  • Quality Control: QC of the raw FASTQ data
  • Sequence Alignment: BAM file, Data Summarization, IGV Visualization
  • Customerized data analysis
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