NGS Services à la carte
Instruments in our fleet
Long-read sequencing technologies
BTSeq™ Contiguous Sequencing Service
Microbial genome analysis
RNASeq and differential gene expression analysis
Tailed amplicon sequencing
Whole exome sequencing
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Use only the sequencing capacity you really need
When ordering Illumina sequencing you can choose one of the following options:
| You order | Sequencing lane | ShareSeq data package |
| What is the service suitable for? | Rather larger projects with a lower price per unit of data (eg one million reads) | Rather small to medium projects with a lower total cost |
| Available sequencing settings | Single-end 50b Paired-end 150b, 250b |
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| Capacity | 300+ million reads | 1+ million reads |
| Guarantee | The amount of data output is approximate. | If library prep is being made in our lab, we guarantee the amount of data specified for ShareSeq data packages! |
| Library preparation | We or you | |
| Library type | No limits | |
| Adapters | Compatible with standard Illumina sequencing primers. | |
| Indexes | Exclusively dual indexes. If you prepare libraries yourself and do not want / cannot use dual indexes, always contact us first. | |
| Outputs | Standard (commonly used data formats etc.) | |
Technical specs and prices of lanes and data packages here.
Lane or data package?The sample processing is identical. Primarily, Share data packages are suitable for small to medium scale projects where a relatively low sequencing capacity per sample is required and it is not worth paying for full-lane sequencing. At the same time, we strongly recommend ShareSeq when you perform large and costly sequencing projects and want to run a low-cost test of, for example, ribo-depletion or other way of target enrichment for a specific genome / transcriptome fraction, reference sequence mapping rate, presence of expected organisms, etc. For ShareSeq data packages, your samples will be analyzed along with samples from other clients. If you prepare the sequencing libraries yourself, it is absolutely critical that you provide us with accurate information on the preparation process, the indexes used, etc. This information will be requested when placing an order in our system. As templates, you can supply any template (DNA / RNA) that can be processed by standard library preparation procedures according to our price list. Libraries will be prepared by our standard protocols and pooled to get the desired output (number of reads). |
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In the case of Illumina technology, we offer the preparation of the following types of libraries:
If you want to prepare the libraries yourself, you must send them to us as one pool. Before sequencing, we always perform a quality check of the libraries prepared by you.
The reads obtained will be sorted according to the combination of indexes into files representing individual samples and analysis of sequencing quality indicators such as number and length of sequences, phred score,% GC, duplication level, etc. will be performed. As output you will receive data in FASTQ format divided into files according to individual samples. This Basic Data Analysis is an integral part of the sequencing and is free.
For some types of analyzes, eg when sequencing exomes, we offer additional standard processing of results. This Advanced Data Analysis is charged based on the number of samples and is optional. If you are not interested in it, you will only receive FASTQ files (above).
Because each sequencing project has specific data analysis requirements, we offer turnkey data analysis for the needs of your project - Custom Data Analysis. Our bioinformaticians can help you with any data analysis goal. If you are interested in this service, individual consultation is required, we recommend you seek our help already at the project preparation stage.
Approx. 6 weeks (data analysis not included)
If you are new to NGS, we encourage you to attend our two-day NGS introductory course. We will be happy to welcome you on some of other courses and workshops too.