BioMicroCenter:DNA HTL

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High-throughput DNA Library Preparation

The BioMicro Center offers high-throuhgput DNA library preparation (HTL-DNA) for both intact and fragmented samples as well as for metagenomics/amplicon generation. High-throughput library generation focuses on reducing price and processing time on a per sample basis. To do this, there are several key differences from our standard library preparation service. First, HTL-DNA services have set batch sizes (24 and 96) with fixed price points (i.e. charge for 16 samples will be the as 24 samples; similarly for 80 samples as 96). If under these batch sizes, DO MORE REPLICATES to simultaneously enhance experimental power and reduce price per sample. Some samples may fail and the cost of re-prepping those samples is NOT included in the quoted cost unless re-prep of the entire plate is deemed necessary. Re-preps can be done by hand, but at a higher rate. Second, the HTL option focuses on reducing price and processing time per sample, so some routine services provided with standard library preparation - such as initial and final quality control for all samples, sample arraying, or automatic re-prep of failed samples - are not built in. These services are available as add ons to the original service request.

Reminder: high throughput projects are treated with one condition (PCR cycles, fragmentation time, etc...). They are meant for allowing high replicates of the same samples. High throughput submissions for projects with multiple sub-projects from separate individuals combined on the same plate result in a low success rate due to the different conditions for each sub project. Therefore, htl submissions from multiple projects will tolerate and may expect, failure rates well over 10%.

FRAGMENTED DNA

NEB Ultra II

Parameter General requirements Pre-load requirements SAMPLE INPUT Fragmented DNA (i.e. ChIP-Seq, small PCR amplicons) RANGE OF INPUT 100pg - 75ng Samples all normalized to same concentration in 10µL (100pg/µL - 7.5ng/µL) SUBMISSION VOLUME >10µL 10 mM Tris pH 8.0 Exactly 10µL 10mM Tris pH 8.0 UNIT 24 samples 96 samples PLATE SETUP Samples should be arrayed by column in a 96-well full-skirt plate (Axygen) Samples arrayed by column in 1st quadrant of 384-well hard-shell plate (BioRad) SEQUENCING RECOMMENDATIONS All platforms INDEX AVAILABILITY 112 Unique Dual Indexes 192 Combinatorial Dual Indexes INCLUDED Library preparation Spot check of final libraries ADDITIONAL SERVICES AVAILABLE Sample QC Sample cleaning Sample arraying Sample re-prep N/A SUBMISSION FORM MIT - ilabs External - form PRICING LINK

NEBNext Ultra II is used for standard ligation-mediated PCR based approaches. We have miniaturized the reaction volume to a 1/5th scale that reliably performs on inputs ranging from 10pg to 75ng (recommended minimum of 100pg). The reaction begins with 10µL of normalized sample to which reagents are added. As such, initial submission of clean samples that have been pre-normalized in greater than 10µL of appropriate buffer will hasten sample processing.

INTACT GENOMES

Nextera Flex

Parameter General requirements Pre-load requirements SAMPLE INPUT Intact DNA and large amplicons RANGE OF INPUT 1ng - 50ng Samples all normalized to same concentration in 3µL (330pg/µL - 16.5ng/µL, *higher is better) SUBMISSION VOLUME >10µL 10 mM Tris Buffer Exactly 3µL 10 mM Tris Buffer UNIT 24 samples 96 samples PLATE SETUP Samples should be arrayed by column in a 96-well full-skirt plate (Axygen) Samples arrayed by column in 1st quadrant of 384-well hard-shell plate (BioRad) SEQUENCING RECOMMENDATIONS All platforms except 40SE HiSeq INDEX AVAILABILITY 384 Unique Dual Indexes Combinatorial Dual Indexes not available INCLUDED Library preparation Spot check of final libraries ADDITIONAL SERVICES AVAILABLE Sample QC Sample cleaning Sample arraying Sample re-prep N/A SUBMISSION FORM MIT - ilabs External - form PRICING LINK

Unlike XT, Nextera Flex utilizes bead-linked transposomes (BLT) to tagment and generate libraries from intact DNA samples. These BLTs control sizing during the tagmentation reaction by sterics, producing a much more consistent libraries with larger size distribution which makes it ideal for larger paired-end runs on sequencers. Nextera Flex is currently run at a 1/10th miniaturization scale on the Mosquito HV with a broader dynamic range of input (1ng - 50ng) compared to XT. Nextera Flex self-normalizes at a certain input (if sample concentration is 3ng/µL or greater) and submissions do not have to be normalized so long as that threshold is met. Up to 384 libraries can be multiplexed using Nextera unique dual-indexes (UDI) which helps to avoid issues with 'barcode hopping'.

Nextera XT

Parameter General requirements Pre-load requirements SAMPLE INPUT Intact DNA and large amplicons RANGE OF INPUT > 0.2ng/µL Samples normalized to 0.2ng/µL SUBMISSION VOLUME >10µL 10 mM Tris Buffer Exactly 5µL 10 mM Tris Buffer UNIT 24 samples 96 samples PLATE SETUP Samples should be arrayed by column in a 96-well full-skirt plate (Axygen) Samples arrayed by column in 1st quadrant of a 384-well LVSD plate (Available at BMC) SEQUENCING RECOMMENDATIONS 40SE HiSeq INDEX AVAILABILITY 16 Unique Dual Indexes 384 Combinatorial Dual Indexes INCLUDED Library preparation Spot check of final libraries ADDITIONAL SERVICES AVAILABLE Sample QC Sample cleaning Sample arraying Sample re-prep N/A SUBMISSION FORM MIT - ilabs External - form PRICING LINK

Nextera XT is a solution-based "tagmentation" chemistry used for the preparation of intact DNA samples to generate libraries with smaller insert sizes which is best suited for 40bp single-end runs on sequencers. Nextera XT has been miniaturized to a 1/12th reaction volume on our Mosquito HV from minimal low sample concentration (0.2ng/µL or greater) and up to 384 libraries can be run on a single sequencing lane using dual indexes. The Mosquito HV allows for libraries to be prepared at decreased volumes which results in significantly reduced costs but also lowers library complexity. As such, it is most suitable for single cell and amplicon analysis. De novo work should not be done using Nextera XT preps on the Mosquito HV.

16S / AMPLICON SEQUENCING

16S Metagenomic/Amplicon Library Preparation Parameter General requirements SAMPLE INPUT Clean DNA RANGE OF INPUT As available SUBMISSION VOLUME >10µL 10 mM Tris Buffer UNIT 48 samples* The BioMicro Center strongly encourages leaving space for 4 control samples within each batch of 48. PLATE SETUP Samples should be arrayed by column from left to right in a 96-well full-skirt plate (Axygen) SEQUENCING RECOMMENDATIONS 250PE/300PE MiSeq INDEX AVAILABILITY 16 Unique Dual Indexes 96 Combinatorial Dual Indexes INCLUDED Initial qPCR Library preparation Spot check of final libraries ADDITIONAL SERVICES AVAILABLE Sample QC Sample cleaning Sample arraying SUBMISSION FORM MIT - ilabs External - form PRICING LINK

16S v4 region amplified in standard BioMicro Center preps. Other regions can be substituted by submitting oligos with different variable regions The BioMicro Center offers 16S and amplicon sequencing for metagenomics projects. Derived from the Alm Lab with support from a pilot grant from MIT CEHS, our protocol uses a two step amplification to first expand the 16S population and add defined 3' and 5' sequences which are then used to add Illumina anchors and sequences. This two step method allows easy multiplexing and the ability change the amplicon insert sequence at minimal cost. The same method used for 16S is also applicable to other amplicons as well with minor adaption. Because we use a nested PCR, only the internal sequences need to be modified. The adapter sequences - Green:Blue - are the key element of this method. On the 5' end, they contain a "YRYR" sequence that introduces the complexity required for Illumina sequencing. FORWARD: ACACGACGCTCTTCCGATCTYRYRXXXXXXX REVERSE: CGGTCTCGGCATTCCTGCTGAACCGCTCTTCCGATCTXXXXXXX (X = insert element) Regions Target Region Forward Primer Reverse Primer Standard Region 16S V4 Primer ID: U515F GTGCCAGCMGCCGCGGTAA Primer ID: E786R GGACTACHVGGGTWTCTAAT Alternative Regions 16S V1-V3 Primer ID: U24F GAGTTTGATYMTGGCTCAG Primer ID: U553R GCGGCTGCTGGCACG 18S - - The most common source of failures for amplicon sequencing are samples that fail to amplify in the initial qPCR. The first step of the process is a qPCR reaction using the forward and reverse primers of the specific target regions to determine the number of cycles to be used in library generation. Libraries that fail to amplify in 20 cycles generally perform poorly enough to be unusable. Removal of PCR inhibitors is critical to success of this protocol. We do attempt to do this by serially diluting the samples and testing dilutions in the initial qPCR.

USEFUL INFORMATION

DNA Pre-load Submissions

Describes samples that upon submission to the BMC can be immediately plugged into the preparatory method that has been specified in the project submission form. This option is provided to reduce library preparation costs and expedite sample processing by minimizing hands-on time by a BMC staff. The specific requirements are listed for each preparatory method (excluding 16S) in the tables above. These specifications must be met in order to qualify as a pre-load, submissions otherwise may be subject to additional charges.

Due to the nature of a pre-load submission, the entire volume of sample submitted will be used and as such, additional services are not typically offered unless coordinated with a BMC technician. It is important to keep this in mind when submitting precious samples and the BMC recommends to save a portion of sample when possibly.

Quadrant Layout

At the BioMicro Center, we organize our high-throughput projects in 384-well plates using a quadrant layout. With quadrant 1 (Q1) representing one 96-well plate, quadrant 2 (Q2) representing a second 96-well plate and so on up to Q4. We ask that plates being submitted start with Q1 and arrayed column-wise. Below are diagrams illustrating quadrant layouts.

Quadrant layout

Quadrant 1 of 384-well plate

Normalization

Normalization is referring to bringing all samples to a uniform concentration. For library preparation, uniform input mass is necessary for proper library generation and as such, calculations for normalization should be based upon concentration in ng/µL. This is in contrast to normalization for pooling of final libraries, where calculations are based upon concentration in nM since the number of molecules is important to achieve a desired read distribution when sequencing.

Unique versus Combinatorial Dual Indexing

Combinatorial dual indexing is a technique that uses a set of Index 1 (denoted as i7) and Index 2(denoted as i5) barcodes that are combined in a manner such that it produces distinct i7 and i5 pairs which increases multiplexing capacity for sequencing. With combinatorial dual indexes, each i7 and i5 is shared among other samples on the same plate, typically with i5's repeating across rows and i7's down columns. These combinations are unique but individual indexes used are not. However, a phenomenon known as 'index hopping' has been observed when sequencing multiplexed libraries that followed single or combinatorial indexing schemes with newer Illumina platforms utilizing ExAmp chemistry such as the NovaSeq (Costello et al., 2018). This swapping of indexes causes reads to be mis-assigned and subsequently excluded from further analysis. The primary strategy employed to mitigate the effects of index hopping is through the utilization of unique dual indexes.

Unique dual indexes (UDI) are non-redundant indexes where each i5 and i7 has a distinct index sequence. As opposed to combinatorial dual indexing, an i7 and i5 index is never repeated nor shared among other samples (i.e. for a 96-well UDI index plate, there are 96 unique i7's and 96 unique i5's). Both the combinations and individual indexes used are unique, and as a result the frequency of mis-assigned reads due to index hopping is greatly reduced. The BioMicro Center recommends that UDI's always be used when sequencing on the NovaSeq. The number of libraries that can be multiplexed and sequenced on a single lane is determined by the total number of UDI's provided for each library preparation method.