# Importing Feature Barcoding Data

* [Create a new Project](#create-a-new-project)
* [Import data](#import-data)

## Create a new Project

Let's start by creating a new project.

* On the *Home page*, click **New project** (Figure 1)
* Give the project a name
* Click **Create project**

![Figure 1. Create a new project and give it a meaningful name (e.g. CITE-Seq tutorial)](/files/LlBkIK4xkvctbPAP6mmj)

## Import data

* In the Analyses tab, click **Add data**
* Click **10x Genomics Cell Ranger counts h5** (Figure 2)
* Choose the filtered HDF5 file for the MALT sample produced by Cell Ranger

![Figure 2. Import options for CITE-Seq tutorial data](/files/ymaAqBF3g9p98vVTrV3G)

Move the .h5 file to where Partek Flow is installed using ![](/files/vxKKv51qniTOjIlzV2Z8), then browse to its location.

![Figure 3. Import options for CITE-Seq tutorial data](/files/GwHtm1xVshsRys0JKtAW)

Note that Partek Flow also supports the feature-barcode matrix output (barcodes.tsv, features.tsv, matrix.mtx) from Cell Ranger. The import steps for a feature-barcode matrix are identical to this tutorial.

* Click **Next**
* Name the sample **MALT** (the default is the file name)
* Specify the annotation used for the gene expression data (here, we choose **Homo sapiens (human) - hg38** and **Ensembl Transcripts release 109**). If Ensembl 109 is not available from the drop-down list, choose **Add annotation** and download it.
* Check **Features with non-zero values across all samples** in the *Report* section
* Click **Finish** (Figure 3)

![Figure 4. File format options for MALT data set](/files/Vt2rcbTXfu19SY7xh8EY)

A *Single cell counts* data node will be created under the *Analyses* tab after the file has been imported. We can move on to processing the data.

## Additional Assistance

If you need additional assistance, please visit [our support page](http://www.partek.com/support) to submit a help ticket or find phone numbers for regional support.


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