The Epigenomics Shared Facility (ESF) is a part of Einstein’s Center for Epigenomics and an Illumina CSPro (certified service provider) laboratory. The high-throughput molecular technological resources in the ESF include massively parallel sequencing (MPS) platforms: the Oxford Nanopore MinION, Illumina NEXTSeq500, Illumina HiSeq2500 and Illumina MiSeq; supported by TECAN freedom Evo® 200 Robotics. The core facility space is dedicated and customized, with MPS library preparation performed in a positive-pressure room isolated from the post prep and sequencing room. The MPS machines are connected by high-bandwidth networking to dedicated computing equipment located in a server room.
Sample submission is coordinated through a laboratory information management system (LIMS) component of the WASP (an integrated LIMS and batch processing system: http://waspsystem.einstein.yu.edu). WASP allow users for electronic submission of their samples, real-time follow-up of the pipeline and access to the data once available. The facility has a turnaround of 2 to 3 weeks per library/job/project. The data is backed-up and available for at least 6 months on the WASP server from the Albert Einstein College of Medicine.
The ESF supports diverse assays for MPS analysis and strives to bring cutting-edge technologies to benefit the programs of Einstein researchers. Recently, with the current COVID-19 pandemic, ESF is ready to facilitate and support your research into the SARS-CoV-2 and the search for effective diagnostics and therapies to cure COVID-19. Please check the Epigenomics Shared Facility -COVID-19 overview for details.
A. The ESF is now providing support and services for long read sequencing utilizing Oxford Nanopore’s MinION platform.
B. Support for diverse assays for short read sequencing to study the epigenome include:
The services include library preparation and sequencing plus Data Storage, primary data return, analysis and visualization through WASP (http://waspsystem.einsteinmed.edu). DNA/RNA isolation services are also provided through Molecular Cytogenetic Facility. We are available on Science Exchange as well.
Secondary analysis is also provided on request through our Computational and Statistical Genomics/Epigenomics Groups (http://wasp.einstein.yu.edu/index.php/AnalysisRequest). We are available on Science Exchange as well. Pricing information is also available through WASP: http://waspsystem.einsteinmed.edu/ws/auth/sequencingPricing.do.
Scientific Director
John M. Greally, M.B., Ph.D.
Operations Director
Shahina B. Maqbool, Ph.D.
Hours | Location |
M-F, 9-5 |
Price Center, Room 159 |
*Please acknowledge the Research Resource Identifiers (RRIDs) SCR_023284 in any publication that was supported by use of this shared resource.*
Name | Role | Phone | Location | |
---|---|---|---|---|
Shahina B. Maqbool, Ph.D. |
Operations Director
|
718.678.1163
|
shahina.maqbool@einsteinmed.edu
|
Price Center 159
|
Service list |
► Assays (111) | |||
Name | Description | Price | |
---|---|---|---|
Alloseq TX17-24 samples-2x150 bp Miseq Micro Flow Cell | Inquire | ||
ATAC-seq - 2 samples - 2x75 bp-60M | Inquire | ||
ATAC-seq - 8 samples - 2x75 bp-20M | Inquire | ||
ATAC-seq -10 samples - 2x150 bp-40M | Inquire | ||
ATAC-seq -10 samples - 2x75 bp-40M | Inquire | ||
BGE-seq-40 samples-2x150 bp | Inquire | ||
CHIP - seq - 8 samples - 2x150 bp-20M | Inquire | ||
CHIP-seq - 10 samples - 1x150 bp or 2x75 bp-30M | Inquire | ||
CHIP-seq - 16 samples -1x150 bp or 2x 75 bp-30M | Inquire | ||
CHIP-seq - 18 samples -1x150 bp or 2x 75 bp-20M | Inquire | ||
CHIP-seq - 4 samples -1x150 bp or 2x75 bp-30M | Inquire | ||
CHIP-seq - 8 samples - 1x150 bp or 2x75 bp-30M | Inquire | ||
CHIP-seq - 8 samples - 2x75 bp or 1x150 bp-20M | Inquire | ||
CHIP-seq-18 samples- 2x150 bp 20M | Inquire | ||
CHIP-seq-18 samples-1x100 bp or 2x50 bp 20M | Inquire | ||
Custom target enrichment-cfDNA- 2x 100 bp with UMI-bulk | Inquire | ||
Cut & Run - seq - 24 samples - 2x35 bp-15M | Inquire | ||
Cut & Run - seq - 3 samples - 2x25 bp-5M | Inquire | ||
Cut & Run - seq - 3 samples - 2x35 bp-50M | Inquire | ||
Cut & RUN-Seq-library prep using cells or nuclei or Chromatin | Inquire | ||
Cut& RUN-Seq-library prep only using DNA | Inquire | ||
Cut&Run-seq-4 samples-2x35 bp-30M | Inquire | ||
Cut&Run-seq-48 samples-2x35 bp-15M | Inquire | ||
ExomeAccess RNASeq-12 samples-2x75 bp-30M | Inquire | ||
HELP-GT - 20-24 samples - 1x50 bp-20M | Inquire | ||
MeDIP/HMeDIPSeq - 12 sample - 2x150 bp-30X | Inquire | ||
MinION Oxford Nanopore Sequencing Only-per Flow Cell | Inquire | ||
Miseq run for Micro Kit - 2x150 bp | Inquire | ||
Miseq run for Nano Kit - 2x250 bp | Inquire | ||
NEB Enzymatic Methyl Seq Library prep only | Inquire | ||
Seq Cap EpI Human - 12 sample - 2x150 bp-30X | Inquire | ||
Seq Cap EpI Human - 8 sample - 2x75 bp-30X | Inquire | ||
Seq Cap EpI mouse - 12 sample - 2x150 bp-30X | Inquire | ||
Shotgun metagenomics sequencing-20 samples- 2x150 bp-20M | Inquire | ||
Small RNA-seq - 16 samples - 1x75 bp-25M | Inquire | ||
Small RNA-seq - 24 samples - 1x75 bp-10M | Inquire | ||
Transcriptome Profiling - 12 samples - 1x150 bp or 2x75 bp-30M | Inquire | ||
Transcriptome Profiling - 12 samples - 1x150 bp or 2x75 bp-30M (60 samples project) | Inquire | ||
Transcriptome Profiling - 12 samples - 1x75 bp-30M (60 samples) | Inquire | ||
Transcriptome Profiling - 12 samples - 2x150 bp-30M (60 samples project) | Inquire | ||
Transcriptome Profiling - 24 samples - 1x75 bp-30M | Inquire | ||
Transcriptome Profiling - 24 samples - 2x150 bp-40M | Inquire | ||
Transcriptome Profiling - 24 samples - 2x75 bp-30M | Inquire | ||
Transcriptome Profiling - 40 samples - 1x75 bp-30M | Inquire | ||
Transcriptome Profiling - 6 samples - 1x150 bp or 2x75 bp 30M | Inquire | ||
Transcriptome Profiling - 6 samples 1x150 bp or 2x75 bp-15M | Inquire | ||
Transcriptome Profiling - 6 samples 1x150 bp or 2x75 bp-60M | Inquire | ||
Transcriptome Profiling - 7 samples - 1x75 bp-50M | Inquire | ||
Transcriptome Profiling - 8 samples - 2x75 bp-20M | Inquire | ||
Transcriptome Profiling - 80 samples - 1x75 bp-30M | Inquire | ||
Transcriptome Profiling - 96 samples - 1x150 bp or 2x75 bp 30M | Inquire | ||
Transcriptome Profiling - 96 samples - 1x75 bp-30M | Inquire | ||
Transcriptome Profiling-3 samples-2x150bp-40M | Inquire | ||
Transcriptome Profiling-3 samples-2x75bp or 1x150 bp-50M | Inquire | ||
Transcriptome Profiling-8 samples-2x150bp-20M | Inquire | ||
Ultra Low RNAseq - Low Input (~100 ng) - 96 samples - 1x75 bp-30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 14 samples - 2x150 bp-30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 14 samples - 2x75 or 1x150 bp-30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 4 samples - 1x100 bp-P1 -25M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 6 samples - 2x75 or 1x150 bp-30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 8 samples - 2x75 or 1x150 bp-30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 9 samples - 1x150 bp or 2x75 bp- 40M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 9-10 samples - 2x150 bp 40M | Inquire | ||
Using cells-Cut&Run-seq-48 samples-2x75 bp-15M | Inquire | ||
Using processed DNA-Cut&Run-seq-48 samples-2x75 bp-15M | Inquire | ||
Whole Exome Sequencing Rodent - 8 samples - 2x150 bp-30X | Inquire | ||
Whole Exome Sequencing Rodent - 8 samples - 2x75 bp-30X | Inquire | ||
Whole Genome Sequencing Small Genome - 8 samples - 2x150 bp-30X | Inquire | ||
ATAC-seq - 4 samples - 2x75 bp-40M | Inquire | ||
ATAC-seq - 8 samples - 2x150 bp-20M | Inquire | ||
CHIP-seq - 12 samples - 1x150 bp-12M | Inquire | ||
CHIP-seq - 12 samples - 1x150 bp-30M | Inquire | ||
CHIP-seq - 24 samples - 1x150 bp-20M | Inquire | ||
HELP-GT - 12 samples - 1x50 bp-5M | Inquire | ||
HELP-GT - 18 samples - 1x50 bp-5M | Inquire | ||
HELP-tag - 12 samples - 1x50 bp-5M | Inquire | ||
Seq Cap Epi Human - 8 samples - 2x150 bp-30X | Inquire | ||
Seq Cap Epi Mouse - 8 samples - 2x150 bp-30X | Inquire | ||
Small RNA-seq - 6 samples - 1x50 bp-20M | Inquire | ||
Small RNA-seq - 9 samples - 1x50 bp-12M | Inquire | ||
Small RNA-seq - 12 samples - 1x50 bp-10M | Inquire | ||
Small RNA-seq - 16 samples - 1x50 bp-7.5M | Inquire | ||
Small RNA-seq - 24 samples - 1x50 bp-10M | Inquire | ||
Transcriptome Profiling - 4 samples - 1x150 bp-30M | Inquire | ||
Transcriptome Profiling - 6 samples - 1x75 bp-60M | Inquire | ||
Transcriptome Profiling - 6 samples - 2x150 bp-30M | Inquire | ||
Transcriptome Profiling - 8 samples - 1x75 bp-40M | Inquire | ||
Transcriptome Profiling - 8 samples - 1x150 bp or 2x75 bp 40M | Inquire | ||
Transcriptome Profiling - 8 samples - 2x150 bp 40M | Inquire | ||
Transcriptome Profiling - 9 samples - 1x150 bp 40M | Inquire | ||
Transcriptome Profiling - 9 samples - 2x150 bp 40M | Inquire | ||
Transcriptome Profiling - 10 samples - 1x75 bp-40M | Inquire | ||
Transcriptome Profiling - 12 samples - 1x75 bp-30M | Inquire | ||
Transcriptome Profiling - 12 samples - 1x150 bp or 2x75 bp 30M | Inquire | ||
Transcriptome Profiling - 12 samples - 2x150 bp 30M | Inquire | ||
Transcriptome Profiling - 16 samples - 1x75 bp-30M | Inquire | ||
Transcriptome Profiling - 16 samples - 1x150 bp or 2x75 bp-30M | Inquire | ||
Transcriptome Profiling -16 samples 2x150 bp-30M | Inquire | ||
Transcriptome Profiling - 96 samples - 2x150 bp-30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 2 samples - 1x150 bp 40M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 2 samples - 2x150 bp 30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 6 samples - 1x75 bp-60M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 6 samples - 2x150 bp-30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 9 samples - 1x150 bp 40M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 12 samples - 1x75 bp 30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 12 samples - 1x150 bp 30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 12 samples - 2x150 bp 30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 16 samples - 1x75 bp-30M | Inquire | ||
Whole Genome BS - 8 samples - 2x150 bp | Inquire | ||
Whole Genome Sequencing Human - 1 sample - 2x150 bp-30X | Inquire | ||
Whole Genome Sequencing Rodent - 1 sample - 2x150 bp-30X | Inquire | ||
► Illumina MiSeq Sequencing Services (13) | |||
Name | Description | Price | |
MiSeq 1x 75 bp or 1x100 bp | Inquire | ||
Miseq run for Nano Kit-2x150 bp | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 4 samples - 2x150 bp-(Micro-Miseq ) | Inquire | ||
MiSeq 1x200 bp | Inquire | ||
MiSeq 1x50bp | |||
MiSeq 1x150bp | |||
MiSeq 1x250bp | Inquire | ||
MiSeq 1x300bp | |||
MiSeq 2x25bp | |||
MiSeq 2x75bp | |||
MiSeq 2x150bp | |||
MiSeq 2x250bp | |||
MiSeq 2x300bp | |||
► Illumina HiSeq 2500 Sequencing Services (2) | |||
Name | Description | Price | |
HiSeq 2500 1x50bp | |||
HiSeq 2500 1x150bp | |||
► Automated Library Preparation For Massively Parallel Sequencing (24) | |||
Name | Description | Price | |
Amplicon Sequencing / Batch 1: 1-16 samples |
Sample Type: PCR amplified DNA in batches |
||
Amplicon Sequencing / Batch 2: 17-32 samples |
Sample Type: PCR amplified DNA in batches |
Inquire | |
Amplicon Sequencing / Batch 3: 33-48 samples |
Sample Type: PCR amplified DNA in batches |
Inquire | |
Amplicon Sequencing / Batch 4: 49-64 samples |
Sample Type: PCR amplified DNA in batches |
Inquire | |
Amplicon Sequencing / Batch 5: 65-80 samples |
Sample Type: PCR amplified DNA in batches |
Inquire | |
Amplicon Sequencing / Batch 6: 81-96 samples |
Sample Type: PCR amplified DNA in batches |
Inquire | |
Resequencing (whole genome, exome, targeted) / Batch 1: 1-16 samples |
Sample Type: Genomic DNA in batches |
Inquire | |
Resequencing (whole genome, exome, targeted) / Batch 2: 17-32 samples |
Sample Type: Genomic DNA in batches |
Inquire | |
Resequencing (whole genome, exome, targeted) / Batch 3: 33-48 samples |
Sample Type: Genomic DNA in batches |
Inquire | |
Resequencing (whole genome, exome, targeted) / Batch 4: 49-64 samples |
Sample Type: Genomic DNA in batches |
Inquire | |
Resequencing (whole genome, exome, targeted) / Batch 5: 65-80 samples |
Sample Type: Genomic DNA in batches |
Inquire | |
Resequencing (whole genome, exome, targeted) / Batch 6: 81-96 samples |
Sample Type: Genomic DNA in batches |
Inquire | |
RNA Sequencing - Low Input (~100 ng) / Batch 1: 1-16 samples |
Sample Type: Low input RNA samples in batches |
Inquire | |
RNA Sequencing - Low Input (~100 ng) / Batch 2: 17-32 samples |
Sample Type: Low input RNA samples in batches |
||
RNA Sequencing - Low Input (~100 ng) / Batch 3: 33-48 samples |
Sample Type: Low input RNA samples in batches |
||
RNA Sequencing - Low Input (~100 ng) / Batch 4: 49-64 samples |
Sample Type: Low input RNA samples in batches |
Inquire | |
RNA Sequencing - Low Input (~100 ng) / Batch 5: 65-80 samples |
Sample Type: Low input RNA samples in batches |
||
RNA Sequencing - Low Input (~100 ng) / Batch 6: 81-96 samples |
Sample Type: Low input RNA samples in batches |
Inquire | |
RNA Sequencing / Batch 1: 1-16 samples |
Sample Type: Total RNA samples in batches |
Inquire | |
RNA Sequencing / Batch 2: 17-32 samples |
Sample Type: Total RNA samples in batches |
Inquire | |
RNA Sequencing / Batch 3: 33-48 samples |
Sample Type: Total RNA samples in batches |
||
RNA Sequencing / Batch 4: 49-64 samples |
Sample Type: Total RNA samples in batches |
||
RNA Sequencing / Batch 5: 65-80 samples |
Sample Type: Total RNA samples in batches |
||
RNA Sequencing / Batch 6: 81-96 samples |
Sample Type: Total RNA samples in batches |
||
► Library Preparation For Massively Parallel Sequencing (9) | |||
Name | Description | Price | |
Amplicon Sequencing |
Sample Type: PCR Amplified DNA |
Inquire | |
ATAC-Seq (genome-wide factor occupancy-epigenomic profiling of open chromatin) |
Sample Type: Fresh Cells (500-50,000) |
Inquire | |
ChIP-Seq |
Sample Type: Immunoprecipitated chromatin and input DNA |
Inquire | |
Custom Design Library Prep |
Variable price dependent on customization needed. |
Inquire | |
De Novo Assembly (mate pair library) |
Sample Type: Genomic DNA |
Inquire | |
Directional RNA-Seq |
Sample Type: Total RNA |
Inquire | |
HELP Tagging (genome-wide methylation profiling) |
Sample Type: Genomic DNA |
Inquire | |
miRNA-Seq |
Sample Type: Total RNA |
Inquire | |
Resequencing (whole genome, exome, targeted) |
Sample Type: Genomic DNA |
Inquire | |
► NextSeq Sequencing Services (7) | |||
Name | Description | Price | |
NextSeq 500 HO 1x75bp SE |
Up to 400 M reads |
Inquire | |
NextSeq 500 HO 1x150bp SE |
Up to 400 M reads |
Inquire | |
NextSeq 500 HO 2x75bp PE |
Up to 400 M reads |
Inquire | |
NextSeq 500 HO 2x150bp PE |
Up to 400 M reads |
Inquire | |
NextSeq 500 MO 1x150bp SE |
130 M reads |
Inquire | |
NextSeq 500 MO 2x75bp PE |
130 M reads |
Inquire | |
NextSeq 500 MO 2x150bp PE |
130 M reads |
Inquire | |
► Multiplexing Charges (6) | |||
Name | Description | Price | |
Multiplexing / 1-4 samples, cost/lane | |||
Multiplexing / 5-8 samples, cost/lane | |||
Multiplexing / 9-12 samples, cost/lane | |||
Multiplexing / 13-24 samples, cost/lane | |||
Multiplexing / 25-48 samples, cost/lane | |||
Multiplexing / 49-96 samples, cost/lane | |||
► WASP (1) | |||
Name | Description | Price | |
WASP Data Analysis | Inquire | ||
► Custom Design Target Capture Sequencing (6) | |||
Name | Description | Price | |
Custom Design, 1-sample/capture |
Customer/user provides Choice Libraries (purchased fully by user) to use for capturing/enrich customer regions of interest. We recommend SeqCap EZ Choice Libraries (NimbleGen) to enrich customer regions of interest available in various sizes up to 50 Mb for human and other genomes. We also recommend to pool multiple samples to capture in one reaction however, it is users choice to decide the number of samples (libraries) to be pooled depending upon the desired fold coverage and the size of the target region. |
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Custom Design, 2-samples/capture | |||
Custom Design, 3-samples/capture | |||
Custom Design, 4-samples/capture | |||
Custom Design, 6-samples/capture | |||
Custom target enrichment-Bulk-User provide all reagents | Inquire | ||
► SeqCap Epi (1) | |||
Name | Description | Price | |
SeqCap Epi Choice |
The SeqCap Epi Choice assays are customized, utilizes selective probe pools that can target both strands of bisulfite treated human genomic DNA for targets up to 90Mb. We provide this service as project based please consult ESF about your project needs. |
Inquire | |
► Adaptors and Primers (3) | |||
Name | Description | Price | |
HELP TAG TruSEQ Adaptors, 10µM / 20µl aliquots | |||
HELP TAG TruSEQ RT Primer, 10µM / 20µl aliquots | |||
ILLUMINA P5 & P7 Primers, 10µM / 50µl aliquots | |||
► Whole Human Genome Sequencing (1) | |||
Name | Description | Price | |
Shipping & Handling Fee | Inquire | ||
► Other (6) | |||
Name | Description | Price | |
Bioanalyzer QC - High sensitive chips and reagents | Inquire | ||
Covaris Fragmentation | Inquire | ||
Covaris Instrument Use | Inquire | ||
E-gel | Inquire | ||
Quantification (Qubit) | Inquire | ||
Trueseq Primers-Reagents For Library Prep | Inquire | ||
► Archived Services (46) | |||
Name | Description | Price | |
Bioanalyzer Quality Analysis | Inquire | ||
DNA Sequencing with User Provided Reagents | Inquire | ||
Exome-Seq-Human 2x100bp, Capture Cost/4 samples |
We use SeqCap EZ Exome Library v3.0 (NimbleGen) solution-based capture method that enables enrichment of the whole exome and miRNAs, based on the latest database builds and offering a 64 Mb sequence capture. Turnaround time: 6-8 weeks depending upon the number of samples. Note: You must submit minimum of 4 samples to process at one time for ~50X coverage. There are other options also available such as 30X or 100X coverage, please contact ESF for pricing. |
External
$968.00
each
|
|
Exome-Seq-Human 2x100bp, Cost/sample |
We use SeqCap EZ Exome Library v3.0 (NimbleGen) solution-based capture method that enables enrichment of the whole exome and miRNAs, based on the latest database builds and offering a 64 Mb sequence capture. Turnaround time: 6-8 weeks depending upon the number of samples. Note: You must submit minimum of 4 samples to process at one time for ~50X coverage. There are other options also available such as 30X or 100X coverage, please contact ESF for pricing. |
External
$1,554.00
Sample
|
|
Exome-Seq-Human 2x100bp, Library Cost per sample | Inquire | ||
Exome-Seq-Human 2x100bp, Library Cost/4 samples |
External
$1,800.00
each
|
||
Exome-Seq-Human 2x100bp, Paired end sequencing cost/lane/4 samples |
External
$2,850.00
each
|
||
Exome-Seq-Human 2x100bp, Total cost for 4 samples (Library+Capture+Sequencing) |
External
$6,218.00
each
|
||
Exome-Seq-Mouse 2x100bp, Cost/sample |
We use SeqCap EZ Exome Library v3.0 (NimbleGen) solution-based capture method that enables enrichment of the whole exome and miRNAs, based on the latest database builds and offering a 64 Mb sequence capture. Turnaround time: 6-8 weeks depending upon the number of samples. Note: You must submit minimum of 4 samples to process at one time for ~50X coverage. There are other options also available such as 30X or 100X coverage, please contact ESF for pricing. |
External
$1,390.00
each
|
|
Exome-Seq-Mouse 2x100bp, Total cost for 4 samples (Library+Capture+Sequencing) |
External
$5,560.00
each
|
||
Other QC | Inquire | ||
SeqCap Epi CpGiant 2x100bp, Cost/sample |
We provide services for SeqCap Epi, target enrichment of bisulfite treated DNA, to identify genome wide methylation variation assessment (Human), using Roche NimbleGen solution-based capture methods. Turnaround time: 6-8 weeks depending on the number of samples. Note: You must submit a minimum of 3 samples to process at one time for 30x coverage. There are other options also available. Please contact the ESF for further details. |
External
$1,693.00
Sample
|
|
SeqCap Epi CpGiant 2x100bp, Cost/sample - Bulk Project | Inquire | ||
SeqCap Epi CpGiant 2x100bp, Total cost for 3 samples (Library+Capture+Sequencing) |
We provide services for SeqCap Epi, target enrichment of bisulfite treated DNA, to identify genome wide methylation variation assessment (Human), using Roche NimbleGen solution-based capture methods. Turnaround time: 6-8 weeks depending on the number of samples. Note: You must submit a minimum of 3 samples to process at one time for 30x coverage. There are other options also available. Please contact the ESF for further details. |
External
$5,080.00
each
|
|
Size Selection by PippinHT (Sage Science) for MPS Library Prep |
Up to 12 samples per chip. |
Inquire | |
WGBS 2x100bp, Total cost for 1 sample (Library+Sequencing) for up to 5X coverage (~15Gb data) |
Whole-genome bisulfite sequencing (WGBS) for methylation analysis. Turnaround Time: 6-8 weeks depending on the number of samples. |
External
$3,205.00
Sample
|
|
WGBS Total cost for 1 sample (Library+Sequencing) for up to 30X coverage |
Whole-genome bisulfite sequencing (WGBS) for methylation analysis. Turnaround Time: 6-8 weeks depending on the number of samples. |
External
$10,795.00
Sample
|
|
Whole Human Genome Sequencing (30X) / HiSeq X10 at NYGC |
Price is per sample. Please note: shipping and handling costs will also be applied to orders for whole human genome sequencing. |
Inquire | |
HiSeq 2500 1x100bp | |||
ATAC-seq - 4 samples - 2x100 bp-40M | Inquire | ||
MiSeq 1x100bp | Inquire | ||
ATAC-seq - 8 samples - 2x100 bp-40M | Inquire | ||
HiSeq 2500 1x250bp | |||
CHIP-seq - 4 samples -1x150 bp-30M | Inquire | ||
HiSeq 2500 2x50bp | |||
CHIP-seq - 8 samples - 1x150 bp-30M | Inquire | ||
HiSeq 2500 RR 2x50bp | |||
CHIP-seq - 10 samples - 1x150 bp-30M | Inquire | ||
HiSeq 2500 2x100bp | |||
HiSeq 2500 2x150bp | |||
CHIP-seq - 12 samples - 1x100 bp-30M | Inquire | ||
HiSeq 2500 2x250bp | |||
CHIP-seq - 16 samples - 1x100 bp-20M | Inquire | ||
Custom Target Enrichment | Inquire | ||
HiSeq 2500 RR - Full Flow Cell - 2x100bp | Inquire | ||
HiSeq 2500 RR - Full Flow Cell - 2x150 bp | Inquire | ||
Seq Cap EZ (Custom) - 8-10 samples - 2x100 bp-30X | Inquire | ||
Transcriptome Profiling - 6 samples - 1x150 bp-30M | Inquire | ||
Transcriptome Profiling - 12 samples - 1x150 bp >30M | Inquire | ||
Transcriptome Profiling - 96 samples - 2x75 bp-30M | Inquire | ||
Ultra Low RNAseq-Low Input (~100 ng) - 9 samples - 2x150 bp >40M | Inquire | ||
Whole Exome Sequencing Human - 3 samples - 2x100 bp-30X | Inquire | ||
Whole Exome Sequencing Human - 8 samples - 2x100 bp-30X | Inquire | ||
Whole Exome Sequencing Rodent - 8 samples - 2x100 bp-30X | Inquire | ||
Whole Genome Sequencing Rodent - 2 samples - 2x250 bp-30X | Inquire | ||
Whole Genome Sequencing Small Genome - 8 samples - 2x100 bp-30X | Inquire | ||
► NextSeq2K Sequencing Services (6) | |||
Name | Description | Price | |
NextSeq 2000-P1- 1x100 bp or 2x50bp PE-100M | Inquire | ||
NextSeq 2000-P1- 2x300bp PE-100M | Inquire | ||
NextSeq 2000-P2- 2x150bp PE-400M | Inquire | ||
NextSeq 2000-P2- 2x300bp PE-400M | Inquire | ||
NextSeq 2000-P3- 2x100 bp PE-1200M | Inquire | ||
NextSeq 2000-P3- 2x150 bp PE-1200M | Inquire | ||
► Tape Station (15) | |||
Name | Description | Price | |
Tape Station - 4150 - 1 Sample | Inquire | ||
Tape Station - 4150 - 2 Samples | Inquire | ||
Tape Station - 4150 - 3 Samples | Inquire | ||
Tape Station - 4150 - 4 Samples | Inquire | ||
Tape Station - 4150 - 5 Samples | Inquire | ||
Tape Station - 4150 - 6 Samples | Inquire | ||
Tape Station - 4150 - 7 Samples | Inquire | ||
Tape Station - 4150 - 8 Samples | Inquire | ||
Tape Station - 4150 - 9 Samples | Inquire | ||
Tape Station - 4150 - 10 Samples | Inquire | ||
Tape Station - 4150 - 11 Samples | Inquire | ||
Tape Station - 4150 - 12 Samples | Inquire | ||
Tape Station - 4150 - 13 Samples | Inquire | ||
Tape Station - 4150 - 14 Samples | Inquire | ||
Tape Station - 4150 - 15 Samples | Inquire |