Frequently Asked Questions

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General FAQs

Shoreline Biome kits are currently available for research use only and are not for redistribution. If you are interested in using Shoreline Biome kits for diagnostic assay development, please contact us at support@shorelinebiome.com

We do not, but stay tuned for updates! Subscribe to our newsletter here.

Shoreline Biome assay kits can be purchased via credit card or purchase order from our secure online store. For quotes and larger orders, please email orders@shorelinebiome.com.

Unfortunately, our kits have not been validated for Oxford Nanopore at this time. Make sure to subscribe to our newsletter here for updates!

Shoreline Biome kits:

  • provide the most complete and easy-to-use microbiome sequencing solution on the market. Experienced and novice microbiome researchers alike trust Shoreline Biome assay kits for fast, comprehensive data results.
  • allow researchers to quickly generate the amplicons required for their short- or long-read sequencing data provide the highest quality 16S amplicon preps available, prepared for pooling and sequencing on either the Illumina or PacBio sequencing platform. In head-to-head comparisons, Shoreline Biome’s proprietary technology has identified organisms that other kits could not. It is not necessary to weigh samples prior to starting the process.
  • allow for simple lysis of up to 96 samples with comprehensive representation of Gram-positive Firmicutes and other difficult-to-lyse microbes in under 35 minutes. They are configured in a 96-well plate format that provides a seamless transition to single-step PCR.
  • have unique, dual-matched barcode designs that cover known PCR primer variants while limiting PCR bias and maintaining proportional representation.
  • when used with the PacBio platform, Shoreline Biome’s intuitive analysis software and specially curated Athena database allow a straightforward analysis of the sequence data with superior high-resolution readouts.

SBAnalyzer and Athena Database

Yes, please contact support@shorelinebiome.com  for further  instructions.

No, the SBanalyzer will not be able to demultiplex other barcoded amplicons from home brew or other 16S kits.

Yes, but you must have R and SBanalyzer version 3 installed to be able to infer ASVs from your taxa of interest. Demultiplexed FASTQ files from SBanalyzer v3 can be used in DADA2 (https://benjjneb.github.io/dada2/index.html) to infer ASVs from bacteria in samples. For additional instructions please contact support@shorelinebiome.com.

Reference: Callahan BJ, McMurdie PJ, Rosen MJ, Han AW, Johnson AJ, Holmes SP. DADA2: High-resolution sample inference from Illumina amplicon data. Nat Methods. 2016 Jul;13(7):581-3. doi: 10.1038/nmeth.3869. Epub 2016 May 23. PMID: 27214047; PMCID: PMC492737

Yes, expert Linux users can opt to run SBanalyzer from the command line but an X11 server must be installed and running on the Linux system. Please contact support@shorelinebiome.com for further instructions.

  • There is currently no MacOS version of SBanalyzer, but the Centos version of SBanalyzer can be run on Oracle VM VirtualBox, which can be installed on Macintosh computers. Mac must meet hardware specs (contact support@shorelinebiome.com for details).

​Yes, version 2 is still available. Please contact support@shorelinebiome.com to discuss gaining access to prior versions of SBanalyzer.

No, you must use the SBanalyzer software to demultiplex you sample run as it is preset to the dual index barcodes in the Shoreline Biome V1-V9 and StrainID kits.

Yes but you must have a Qiime2 environment, R, and SBanalyzer version 3 installed, and run the ASV Expert User Protocol to produce a ‘.biom’ file and other QIIME-ready files from the ASV results.   After running the Expert User Protocol to generate ASVs, import  your ASV .fasta, .biom, .tax files into QIIME2. The user is required to generate a .tsv file containing relevant sample metadata (time point info, health conditions, treatments, etc). For further information go to https://qiime2.org/

Yes, the SBanalyzer software can be used for V1-V9 and StrainID kits. When setting up the analysis in the software, just be sure to choose the correct dropdown when selecting kit type in the GUI.  Please be aware that while both amplicons can be mapped to the Athena database, strain level resolution is only achievable using the StrainID kit containing the PCR primers to amplify the longer 16S-ITS-23S gene sequences.

The Shoreline Biome StrainID kit is a unique long amplicon that requires mapping to our specially curated Athena database. Athena is built from RefSeq genomes, and contains comprehensive, integrated, non-redundant, well-annotated genomes. Many of these genomes overlap with other databases (i.e., homd, etc). Currently, the database contains sequences from 18,566 genomes, including 77,212 16S-23S regions (SBanalyzer v3.14).

The Athena database contains contiguous 16S-ITS-23S gene sequences from comprehensive, integrated, non-redundant, well-annotated genomes, enabling strain level differentiation for many bacteria. Strain-level taxonomic differentiation of bacteria using 16S databases (SILVA, RDP, Riken, HOMD, etc.) is typically not possible regardless of how many sequences are in the database, because closely related bacteria may share identical,  full-length 16S gene sequences. The Athena database contains the spacer-region sequences between the 16S and 23S genes, which are a rich source of variability crucial for differentiating closely related bacterial strains.

  • SBanalyzer can be installed on computers running Windows 10 or Centos7 or Centos8 OS.
  • Computers below minimum hardware requirements may be useable, but processing can take several days, memory capacity may be exceeded, and drive space may not be sufficient to install Athena and/or SILVA database

Recommended requirements for desktop, standalone server, or laptop:

  • 16 GB RAM (32 GB or greater recommended)
  • Processor Options: Six core i7 4 GHz minimum. 8 core i9 or greater preferred
  • 1 TB disk drive (2 TB or greater preferred)
  • Microsoft Excel for Windows 10, Centos 8 GUI with LibreOffice
  • Can be run on Oracle VM with Centos 8 installed on Mac or Windows machine that meets hardware specs
  • Microsoft Excel for Windows, LibreOffice for CentOS

Shipping

Yes, we have distributors covering regions outside the United States. They can be found here. If you do not see a distributor covering your region, please contact support@shorelinebiome.com.

If you are interested in international distribution, please contact our Business Development team at hello@shorelinebiome.com

Each U.S. customer is provided an estimate of delivery upon confirmation of their order. We normally ship Monday-Thursday via UPS Next Day Air. Orders confirmed on Friday will not be shipped until the following Monday.

Shoreline Complete

Due to the complexity of the barcode-primer sequence and the variabilities in demultiplexing software, we do not suggest combining different library preps in the same sequencing run. 

The following can be pooled together in a single sequencing run. For any other combination, please contact Technical Support at support@shorelinebiome.com.

KitThese sets can be pooled
V4V4 Sets A, B, and C
V1-V3V1-V3 Set A and B
V1-V9V1-V9 Set Z and A, V1-V9 Set Z and StrainID Set Z
StrainIDStrainID Set Z and A, StrainID Set Z and V1-V9 Set Z

Yes, we have used the Invitrogen DynaMag™-96 Side Magnet (Cat. No. 12331D) on Lysis-1 tubes with success.

Yes, you can use the Agilent Bioanalyzer. We typically run a minimum of 96 samples therefore it is not cost-effective to use the Agilent Bioanalyzer for large number of samples. However, if you are testing a small number of samples (i.e. 16 samples), you may want to use it.

Shoreline Complete kits are the complete solution. The kit can lyse, purify, and amplify your sample. A separate extraction kit is not required.

Shoreline Wave kits require 10-100 ng of purified DNA.

Bead beating is not required. Shoreline Complete’s novel lysis eliminates the need for bead beating.

To build our primer sets, we performed a search of the SILVA database (hundreds of thousands of complete and partial 16S genes), the Riken database (2,275 complete and 5,664 draft genome sequences including the Human Microbiome Project (HMP) genome sequences data from NCBI), the Athena database which has 18,566 fully assembled genomes from RefSeq database (Dec. 2018).

The databases include organisms from many different sources including human oral, fecal, skin, model organisms, environment, etc. Our design includes all known (sequenced) variants and prospective unknown primer variants based on the rRNA gene structure. We also have a novel primer design that limits the effects of potential primer depletion or competition.

For lysis, purification, and amplification of 96 samples it takes about half a day.

Find the list below for the number of barcodes available per kit.

Shoreline Complete/Wave KitBarcodes
V4288
V1-V3192
V1-V9112
StrainID112

Yes! Shoreline Biome has the following kits for purchase that support PacBio sequencing.

  • The Shoreline Complete V1-V9 kit supports full-length 16S. It provides reagents for lysis, purification, and amplification. This kit yields SMRTbell-ready amplicons of approximately 1,500 bp. The full-length 16S amplicon generally leads to identification of microbes at the species level.
  • The Shoreline Complete StrainID kit supports 16S-ITS-23S. It provides reagents for lysis, purification, and amplification. This kit yields SMRTbell-ready amplicons of approximately 2,500 bp. The StrainID amplicon allows identification of microbes at the strain level.
  • The Shoreline Wave V1-V9 kit supports full-length 16S. It provides reagents for amplification only. This kit yields SMRTbell-ready amplicons of approximately 1,500 bp. The full-length 16S amplicon generally leads to identification of microbes at the species level.
  • The Shoreline Wave StrainID kit supports 16S-ITS-23S. It provides reagents for amplification only. This kit yields SMRTbell-ready amplicons of approximately 2,500 bp. The StrainID amplicon allows identification of microbes at the strain level.

All kits come in 16-tube or 96-well plate format.

Yes! Shoreline Biome has the following kits for purchase that support Illumina 16S sequencing:

These kits include Illumina sequencing adaptors which are added to the amplicons during the PCR step. Additionally, both kits output 96 barcode-labeled amplicons ready for Illumina sequencing. All kits come in 16-tube or 96-well plate format.

Currently, our kits do not contain the appropriate primers to amplify fungi or viruses so the V1-V9 and StrainID kits cannot but used for this. We do have ongoing development projects for this application and will update our customers to any new products. Subscribe to our newsletter here.

You will need:

  • a magnet for handling the magnetic beads (Invitrogen DynaMag 96 side magnetic rack, #12331D or Magnetic stand-96 #AM10027). Please note that we strongly recommend the Invitrogen DynaMag 96 magnet. We’ve found that users have had the most success with this type of magnet. The Magnetic stand-96 (Thermo Fisher #AM10027) is the only other approved magnet. Plate magnets that have a ‘well’ type magnet rather than a ‘bar’ or ‘post’ will result in low DNA yield.
  • for post PCR clean up, the Qiagen MinElute® PCR Purification Kit (Cat. No. 28004).

other required items common to most labs and are listed in each Technical Manual.

Consensus sequence for V1-V3:

  • 27f AGRRTTYGATYHTDGYTYAG
  • 515r TYACCGCRRCKGCTGGCAC

Consensus sequence for V4:

  • 515F GTGRCAGCKGRRGCGGTYA
  • 806R GGAYTACNVGGGTHTCTAAK

Consensus sequence for V1-V9:

  • 27f AGRRTTYGATYHTDGYTYAG
  • 1492r TASVGHTACCTTGTTACCGACTT

Consensus sequence for Strain ID:

  • 27f AGRRTTYGATYHTDGYTYAG
  • R AGTACYRHRARGGAANGR

Researchers can choose their own microbiome controls. We have several that we’ve used successfully from Zymo and ATCC.

  • Process positive control: ATCC MSA-2002, MSA2006, Zymo D6300
  • Process negative control: water at the lysis step
  • PCR positive control: MSA 1002, MSA1006, Zymo D6305
  • PCR negative control: water at the PCR step

Shoreline Biome recommends including controls in your project to monitor lysis and amplification efficiency, as well as environmental contamination.

The Shoreline Complete kits contain a Lyse & Purify sub-kit and an Amplify sub-kit.

The Lyse & Purify Sub-kit contains:

  • a 96-well plate or 16 tubes for lysis
  • 2 bottles or tubes of DNA purification beads

The Amplify Sub-kit contains:

  • a PCR plate seal for amplification
  • a 96-well PCR plate containing 96 barcoded primers or 16 tubes containing 16 barcoded primers

For Illumina, these primers target either the V1–V3 or V4 region of the 16S rRNA gene. Following PCR amplification, the amplicons containing the Illumina sequencing adaptor are pooled, purified, and are ready for sequencing.

For PacBio, these primers target either the full 16S rRNA gene or the 16S-ITS-23S region. Following PCR amplification, the amplicons are pooled and ready for the PacBio SMRTbell reaction.

This chart below shows the advantages of the various amplicons. Here, we are looking at 137 E. coli strains. E. coli 16S gene is similar for many strains, so even if we target the full 16S sequence (i.e. V1V9) we would only be able to resolve ~50% of the strains. The StrainID kit allows full resolution and identification of all 137 strains.

We developed the V1-V9 kit for customers who have existing data on the full 16S gene but also want the technological benefits of our Shoreline Biome lysis and primers. In addition, there are a few organisms that cannot be detected with the StrainID kit because the primer targets are not located near one another within the genome. Notably, Helicobacter pylori, Deinococcus radiodurans, some members of Phylum Planctomycetes.

Shoreline Biome kits have been optimized for low-sample inputs. Adding too much sample could cause the assay to fail. The following guidelines are recommended for sample input lysis:

Sample TypeInput AmountMaximum
Solid Fecal1-3 mg10 mg
Liquid Fecal10 µL 10 µL
DNA Genotek OMNIgene®•Gut 10 µL 10 µL
Tissue20 mg30 mg
Mouse Fecal5 mg (1/4 pellet)10 mg (1/2 pellet)
Bacterial Cells10^610^8

Buffer Considerations: The Shoreline Rapid Prep and Shoreline Complete lysis step is pH dependent, therefore it is important to follow recommended guidelines for sample input. If sample is stored in buffer with pH < 6.5, 10 µL is the maximum input volume. Adding more than this volume can result in suboptimal lysis and affect downstream results.

Coverage is very dependent on experimental design and goals so each project can have different requirements.

Illumina suggests 100,000 reads/sample for 16S analysis. Many researchers have done much lower reads with good results. We have multiplexed 288 samples using Shoreline Biome V4 kits and sequenced on MiSeq with sufficient coverage.

For PacBio sequencing with the StrainID kit we suggest running ~96 samples on one SMRT cell. This gives sufficient reads/sample to identify bacterial strains present at 1% with reasonable confidence on the Sequel I. In general, more reads will yield greater depth per sample, enabling identification of bacteria present at lower levels in the sample. For highly diverse samples where representation below 1% is needed, more than one Sequel I SMRT cell or a single Sequel II SMRTcell may be advisable.

Customers should use “Procedure & Checklist – Full-Length 16S Amplification SMRTbell® Library Preparation and Sequencing” using the SMRTbell Express Template Prep 2.0. 

To find the protocol, go to https://www.pacb.com/applications/complex-populations/microbial/ then expand the Library & Sample Preparation section (“Learn More +”), and click the link to the 16S amplification and sequencing protocol.

Please note that you will be beginning the procedure with an amplicon pool, not individual amplicons as stated in the PacBio protocol. Begin with “AMPure PB Bead Purification” of the already pooled Shoreline PCR products, then skip the PacBio-specific pooling steps, and rejoin the protocol with “SMRTbell Library Construction”

Shoreline Complete and Shoreline Rapid Prep kits have been validated on a variety of samples, as shown below. The protocol will vary depending on sample type.

We have had success with the following sample types:

  • solid fecal
  • liquid fecal, stored in other buffers
  • DNA Genotek OMNIgene®•GUT
  • tissue Samples
  • mouse fecal pellets
  • swabs
  • saliva
  • pelleted cells

For sample types not listed, please contact support@shorelinebiome.com

V1-V3 region is the region targeted by researchers focused on skin and oral microbiome. Find it in our shop here.

Our primers are specific for bacteria and will not amplify other organisms.

Shoreline Rapid Prep

Yes, we have used the Invitrogen DynaMag™-96 Side Magnet (Cat. No. 12331D) on Lysis-1 tubes with success.

Typically for fecal samples you get 100-1000 ng of single stranded DNA, but this varies by sample type. For more information, contact support@shorelinebiome.com

You will need a magnet for handling the magnetic beads (Invitrogen DynaMag 96 side magnetic rack, #12331D or Magnetic stand-96 #AM10027). Please note that we strongly recommend the Invitrogen DynaMag 96 magnet. We’ve found that users have had the most success with this type of magnet. The Magnetic stand-96 (Thermo Fisher #AM10027) is the only other approved magnet. Plate magnets that have a ‘well’ type magnet rather than a ‘bar’ or ‘post’ will result in low DNA yield. Other required items common to most labs and are listed in the Technical Manual.

Researchers can choose their own microbiome controls. We have several that we’ve used successfully from Zymo and ATCC.

  • Process positive control: ATCC MSA-2002, MSA2006, Zymo D6300
  • Process negative control: water at the lysis step
  • PCR positive control: MSA 1002, MSA1006, Zymo D6305
  • PCR negative control: water at the PCR step

Shoreline Biome recommends including controls in your project to monitor lysis and amplification efficiency, as well as environmental contamination.

The DNA isolated from the Rapid Prep is single stranded DNA and we recommend that this DNA be used for PCR applications only.

The Shoreline Rapid Prep kits contain:

  • a 96-well plate or 16 tubes for lysis
  • 2 bottles or tubes of DNA purification beads

Shoreline Biome kits have been optimized for low-sample inputs. Adding too much sample could cause the assay to fail. The following guidelines are recommended for sample input lysis:

Sample TypeInput AmountMaximum
Solid fecal 1-3 mg10 mg
Liquid fecal 10 µL 10 µL
DNA Genotek OMNIgene®•GUT 10 µL 10 µL
Tissue 20 mg30 mg
Mouse fecal 5 mg (1/4 pellet)10 mg (1/2 pellet)
Bacterial Cells10^610^8

Buffer Considerations: The Shoreline Rapid Prep and Shoreline Complete lysis step is pH dependent, therefore it is important to follow recommended guidelines for sample input. If sample is stored in buffer with pH < 6.5, 10 µL is the maximum input volume. Adding more than this volume can result in suboptimal lysis and affect downstream results.

The Shoreline Biome Rapid Prep kit yields single-stranded DNA (ssDNA).

Shoreline Complete and Shoreline Rapid Prep kits have been validated on a variety of samples, as shown below. The protocol will vary depending on sample type.

We have had success with the following sample types:

  • solid fecal
  • liquid fecal, stored in other buffers
  • DNA Genotek OMNIgene®•GUT
  • tissue Samples
  • mouse fecal pellets
  • swabs
  • saliva
  • pelleted cells

For sample types not listed, please contact support@shorelinebiome.com

Shoreline Wave

Yes. We recommend a 10-100 ng DNA input. However, it should be noted that DNA from other kits will be lower quality than our DNA due to the bead beating process that other kits use. This can affect the ability to get long amplicons from samples especially for StrainID kits.

Due to the complexity of the barcode-primer sequence and the variabilities in demultiplexing software, we do not suggest combining different library preps in the same sequencing run. 

The following can be pooled together in a single sequencing run. For any other combination, please contact Technical Support at support@shorelinebiome.com.

KitThese sets can be pooled
V4V4 Sets A, B, and C
V1-V3V1-V3 Set A and B
V1-V9V1-V9 Set Z and A, V1-V9 Set Z and StrainID Set Z
StrainIDStrainID Set Z and A, StrainID Set Z and V1-V9 Set Z

Yes, you can use the Agilent Bioanalyzer. We typically run a minimum of 96 samples therefore it is not cost-effective to use the Agilent Bioanalyzer for large number of samples. However, if you are testing a small number of samples (i.e. 16 samples), you may want to use it.

Shoreline Complete kits are the complete solution. The kit can lyse, purify, and amplify your sample. A separate extraction kit is not required.

Shoreline Wave kits require 10-100 ng of purified DNA.

To build our primer sets, we performed a search of the SILVA database (hundreds of thousands of complete and partial 16S genes), the Riken database (2,275 complete and 5,664 draft genome sequences including the Human Microbiome Project (HMP) genome sequences data from NCBI), the Athena database which has 18,566 fully assembled genomes from RefSeq database (Dec. 2018).

The databases include organisms from many different sources including human oral, fecal, skin, model organisms, environment, etc. Our design includes all known (sequenced) variants and prospective unknown primer variants based on the rRNA gene structure. We also have a novel primer design that limits the effects of potential primer depletion or competition.

Find the list below for the number of barcodes available per kit.

Shoreline Complete/Wave KitBarcodes
V4288
V1-V3192
V1-V9112
StrainID112

Yes! Shoreline Biome has the following kits for purchase that support PacBio sequencing.

  • The Shoreline Complete V1-V9 kit supports full-length 16S. It provides reagents for lysis, purification, and amplification. This kit yields SMRTbell-ready amplicons of approximately 1,500 bp. The full-length 16S amplicon generally leads to identification of microbes at the species level.
  • The Shoreline Complete StrainID kit supports 16S-ITS-23S. It provides reagents for lysis, purification, and amplification. This kit yields SMRTbell-ready amplicons of approximately 2,500 bp. The StrainID amplicon allows identification of microbes at the strain level.
  • The Shoreline Wave V1-V9 kit supports full-length 16S. It provides reagents for amplification only. This kit yields SMRTbell-ready amplicons of approximately 1,500 bp. The full-length 16S amplicon generally leads to identification of microbes at the species level.
  • The Shoreline Wave StrainID kit supports 16S-ITS-23S. It provides reagents for amplification only. This kit yields SMRTbell-ready amplicons of approximately 2,500 bp. The StrainID amplicon allows identification of microbes at the strain level.

All kits come in 16-tube or 96-well plate format.

Yes! Shoreline Biome has the following kits for purchase that support Illumina 16S sequencing:

These kits include Illumina sequencing adaptors which are added to the amplicons during the PCR step. Additionally, both kits output 96 barcode-labeled amplicons ready for Illumina sequencing. All kits come in 16-tube or 96-well plate format.

Currently, our kits do not contain the appropriate primers to amplify fungi or viruses so the V1-V9 and StrainID kits cannot but used for this. We do have ongoing development projects for this application and will update our customers to any new products. Subscribe to our newsletter here.

You will need for post PCR clean up, the Qiagen MinElute® PCR Purification Kit (Cat. No. 28004). Other required items common to most labs and are listed in each Technical Manual.

Consensus sequence for V1-V3:

  • 27f AGRRTTYGATYHTDGYTYAG
  • 515r TYACCGCRRCKGCTGGCAC

Consensus sequence for V4:

  • 515F GTGRCAGCKGRRGCGGTYA
  • 806R GGAYTACNVGGGTHTCTAAK

Consensus sequence for V1-V9:

  • 27f AGRRTTYGATYHTDGYTYAG
  • 1492r TASVGHTACCTTGTTACCGACTT

Consensus sequence for Strain ID:

  • 27f AGRRTTYGATYHTDGYTYAG
  • R AGTACYRHRARGGAANGR

Researchers can choose their own microbiome controls. We have several that we’ve used successfully from Zymo and ATCC.

  • Process positive control: ATCC MSA-2002, MSA2006, Zymo D6300
  • Process negative control: water at the lysis step
  • PCR positive control: MSA 1002, MSA1006, Zymo D6305
  • PCR negative control: water at the PCR step

Shoreline Biome recommends including controls in your project to monitor lysis and amplification efficiency, as well as environmental contamination.

The Shoreline Wave kits contain:

  • a PCR plate seal for amplification
  • a 96-well PCR plate containing 96 barcoded primers or 16 tubes containing 16 barcoded primers

For Illumina, these primers target either the V1–V3 or V4 region of the 16S rRNA gene. Following PCR amplification, the amplicons containing the Illumina sequencing adaptor are pooled, purified, and are ready for sequencing.

For PacBio, these primers target either the full 16S rRNA gene or the 16S-ITS-23S region. Following PCR amplification, the amplicons are pooled and ready for the PacBio SMRTbell reaction.

This chart below shows the advantages of the various amplicons. Here, we are looking at 137 E. coli strains. E. coli 16S gene is similar for many strains, so even if we target the full 16S sequence (i.e. V1V9) we would only be able to resolve ~50% of the strains. The StrainID kit allows full resolution and identification of all 137 strains.

We developed the V1-V9 kit for customers who have existing data on the full 16S gene but also want the technological benefits of our Shoreline Biome lysis and primers. In addition, there are a few organisms that cannot be detected with the StrainID kit because the primer targets are not located near one another within the genome. Notably, Helicobacter pylori, Deinococcus radiodurans, some members of Phylum Planctomycetes.

Coverage is very dependent on experimental design and goals so each project can have different requirements.

Illumina suggests 100,000 reads/sample for 16S analysis. Many researchers have done much lower reads with good results. We have multiplexed 288 samples using Shoreline Biome V4 kits and sequenced on MiSeq with sufficient coverage.

For PacBio sequencing with the StrainID kit we suggest running ~96 samples on one SMRT cell. This gives sufficient reads/sample to identify bacterial strains present at 1% with reasonable confidence on the Sequel I. In general, more reads will yield greater depth per sample, enabling identification of bacteria present at lower levels in the sample. For highly diverse samples where representation below 1% is needed, more than one Sequel I SMRT cell or a single Sequel II SMRTcell may be advisable.

Customers should use “Procedure & Checklist – Full-Length 16S Amplification SMRTbell® Library Preparation and Sequencing” using the SMRTbell Express Template Prep 2.0. 

To find the protocol, go to https://www.pacb.com/applications/complex-populations/microbial/ then expand the Library & Sample Preparation section (“Learn More +”), and click the link to the 16S amplification and sequencing protocol.

Please note that you will be beginning the procedure with an amplicon pool, not individual amplicons as stated in the PacBio protocol. Begin with “AMPure PB Bead Purification” of the already pooled Shoreline PCR products, then skip the PacBio-specific pooling steps, and rejoin the protocol with “SMRTbell Library Construction”

V1-V3 region is the region targeted by researchers focused on skin and oral microbiome. Find it in our shop here.

Our primers are specific for bacteria and will not amplify other organisms.

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