These samples were run by seq2science v1.2.2, a tool for easy preprocessing of NGS data.
Take a look at our docs for info about how to use this report to the fullest.
- Workflow
- alignment
- Date
- November 06, 2024
- Project
- colin_2024
- Contact E-mail
- slrinzema@science.ru.nl
Report generated on 2024-11-06, 14:02 CET based on data in:
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Change sample names:
General Statistics
Showing 54/54 rows and 14/29 columns.| Sample Name | % Duplication | M Reads After Filtering | GC content | % PF | % Adapter | Insert Size | % Dups | % Mapped | M Total seqs | % Proper Pairs | M Total seqs | Genome coverage | M Genome reads | M MT genome reads |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 18408_CL_RNA12_P5_plusTA_A52 | 32.7% | 44.5 | 50.2% | 94.6% | 0.0% | 214 bp | 39.1% | 100.0% | 43.4 | 100.0% | 38.5 | 0.8 X | 58.9 | 0.6 |
| 18409_CL_RNA11_P5_minusTA_A51 | 30.6% | 46.4 | 50.6% | 94.2% | 0.1% | 208 bp | 37.0% | 100.0% | 45.2 | 100.0% | 39.6 | 0.9 X | 64.1 | 0.7 |
| 18410_CL_RNA10_P4_plusTA_A50 | 27.3% | 44.4 | 50.4% | 95.3% | 0.0% | 213 bp | 32.8% | 100.0% | 43.2 | 100.0% | 38.5 | 0.8 X | 58.6 | 0.5 |
| 18411_CL_RNA9_P4_minusTA_A49 | 35.8% | 46.6 | 49.4% | 97.2% | 0.0% | 214 bp | 41.6% | 100.0% | 45.4 | 100.0% | 40.5 | 0.9 X | 63.1 | 0.5 |
| 18412_CL_RNA8_P3_plusTA_A48 | 47.2% | 40.4 | 50.6% | 95.1% | 0.0% | 200 bp | 54.9% | 100.0% | 39.1 | 100.0% | 34.0 | 0.8 X | 58.6 | 0.5 |
| 18413_CL_RNA7_P3_minusTA_A47 | 41.2% | 39.4 | 51.4% | 94.5% | 0.0% | 196 bp | 48.6% | 100.0% | 38.2 | 100.0% | 33.1 | 0.8 X | 56.3 | 0.5 |
| 18414_CL_RNA6_P2_plusTA_A46 | 38.1% | 41.7 | 50.6% | 94.3% | 0.0% | 200 bp | 45.1% | 100.0% | 40.6 | 100.0% | 35.6 | 0.8 X | 58.4 | 0.6 |
| 18415_CL_RNA5_P2_minusTA_A45 | 27.4% | 41.7 | 49.1% | 95.5% | 0.0% | 212 bp | 32.7% | 100.0% | 40.5 | 100.0% | 36.4 | 0.7 X | 53.8 | 0.7 |
| 18416_CL_RNA4_P1_plusTA_A44 | 47.3% | 47.0 | 49.6% | 95.7% | 0.0% | 196 bp | 54.8% | 100.0% | 45.7 | 100.0% | 41.1 | 0.8 X | 59.6 | 0.7 |
| 18417_CL_RNA3_P1_minusTA_A43 | 31.7% | 45.8 | 49.4% | 95.0% | 0.0% | 207 bp | 37.9% | 100.0% | 44.5 | 100.0% | 39.9 | 0.8 X | 58.4 | 0.7 |
| 18418_CL_RNA2_PBMC_plusTA_A42 | 37.4% | 40.8 | 48.7% | 94.0% | 0.0% | 205 bp | 45.0% | 100.0% | 39.7 | 100.0% | 35.1 | 0.8 X | 57.9 | 0.7 |
| 18419_CL_RNA1_PBMC_minusTA_A41 | 25.3% | 43.3 | 47.0% | 96.8% | 0.0% | 209 bp | 29.5% | 100.0% | 42.1 | 100.0% | 38.6 | 0.7 X | 54.3 | 0.6 |
| 44115_Exp188_MvdB_RNA_1_DMSO_A10 | 35.3% | 61.5 | 46.9% | 98.8% | 0.1% | 261 bp | 41.8% | 100.0% | 60.0 | 100.0% | 54.9 | 1.5 X | 78.4 | 0.4 |
| 44116_Exp188_MvdB_RNA_2_TA_1um_A11 | 49.1% | 50.9 | 49.7% | 98.7% | 0.1% | 291 bp | 57.8% | 100.0% | 49.4 | 100.0% | 44.2 | 1.3 X | 69.2 | 0.5 |
| 44117_Exp188_MvdB_RNA_3_LPS_10ngml_A12 | 49.3% | 50.0 | 47.6% | 98.5% | 0.1% | 251 bp | 57.9% | 100.0% | 48.6 | 100.0% | 44.3 | 1.2 X | 63.8 | 0.4 |
| 44118_Exp188_MvdB_RNA_4_LPSTA_A14 | 42.8% | 53.3 | 46.7% | 98.9% | 0.1% | 280 bp | 51.3% | 100.0% | 51.8 | 100.0% | 46.7 | 1.4 X | 72.2 | 0.5 |
| 44119_Exp188_MvdB_RNA_5_4h_ctrl_A20 | 47.4% | 41.5 | 49.6% | 98.6% | 0.1% | 276 bp | 56.2% | 100.0% | 40.4 | 100.0% | 36.0 | 1.1 X | 57.1 | 0.7 |
| 44120_Exp188_MvdB_RNA_6_4h_triam_A23 | 44.5% | 48.4 | 48.9% | 98.8% | 0.1% | 261 bp | 52.5% | 100.0% | 47.3 | 100.0% | 42.7 | 1.2 X | 64.1 | 0.7 |
| 44121_Exp188_MvdB_RNA_7_4h_LPS_A24 | 52.6% | 58.6 | 49.6% | 98.9% | 0.1% | 234 bp | 61.4% | 100.0% | 57.5 | 100.0% | 52.4 | 1.4 X | 71.6 | 1.2 |
| 44122_Exp188_MvdB_RNA_8_4h_triam__LPS_A25 | 50.5% | 51.2 | 51.4% | 98.6% | 0.1% | 237 bp | 60.3% | 100.0% | 50.1 | 100.0% | 41.9 | 1.6 X | 85.8 | 1.0 |
| 44123_Exp188_MvdB_RNA_9_3d_Ctrl_A27 | 51.5% | 58.5 | 50.0% | 98.5% | 0.1% | 232 bp | 60.7% | 100.0% | 57.3 | 100.0% | 48.4 | 1.8 X | 96.4 | 1.2 |
| 44124_Exp188_MvdB_RNA_10_3d_triam_A28 | 61.3% | 54.4 | 49.3% | 98.9% | 0.1% | 291 bp | 71.1% | 100.0% | 53.3 | 100.0% | 48.3 | 1.4 X | 71.3 | 0.9 |
| 44125_Exp188_MvdB_RNA_11_5d_Ctrl_A29 | 61.3% | 37.8 | 49.9% | 98.6% | 0.1% | 246 bp | 71.1% | 100.0% | 36.9 | 100.0% | 33.1 | 1.0 X | 52.3 | 0.5 |
| 44126_Exp188_MvdB_RNA_12_5d_triam_A30 | 60.3% | 47.1 | 50.5% | 98.6% | 0.1% | 301 bp | 70.4% | 100.0% | 46.2 | 100.0% | 40.9 | 1.3 X | 67.6 | 0.7 |
| 44781_Exp101_MvdB_Medium_A79 | 88.3% | 33.8 | 47.8% | 98.4% | 0.1% | 210 bp | 96.2% | 100.0% | 29.6 | 100.0% | 27.0 | 0.7 X | 37.8 | 0.3 |
| 44782_Exp101_MvdB_PMA_10ngml_A80 | 81.7% | 36.4 | 50.7% | 98.9% | 0.1% | 226 bp | 89.5% | 100.0% | 35.8 | 100.0% | 32.0 | 0.9 X | 48.9 | 0.7 |
| 44783_Exp101_MvdB_Ionomycine_149ngml_A81 | 89.7% | 22.4 | 48.8% | 98.0% | 0.1% | 220 bp | 97.9% | 100.0% | 21.4 | 100.0% | 19.6 | 0.5 X | 27.1 | 0.3 |
| 44784_Exp101_MvdB_LPC_10ngml_A82 | 86.2% | 20.6 | 49.7% | 98.7% | 0.1% | 250 bp | 94.0% | 100.0% | 19.9 | 100.0% | 18.1 | 0.5 X | 26.0 | 0.3 |
| 44785_Exp101_MvdB_TA_1um_A83 | 76.9% | 38.2 | 50.7% | 98.8% | 0.1% | 227 bp | 84.5% | 100.0% | 37.3 | 100.0% | 33.6 | 0.9 X | 48.7 | 0.6 |
| 44786_Exp101_MvdB_PMA10ngml_TA1um_A84 | 84.1% | 24.7 | 47.6% | 98.5% | 0.1% | 246 bp | 91.1% | 100.0% | 22.9 | 100.0% | 21.4 | 0.5 X | 27.0 | 0.3 |
| 44787_Exp101_MvdB_Ionomycine149ngml_TA1um_A26 | 86.9% | 29.3 | 50.0% | 98.7% | 0.2% | 234 bp | 95.1% | 100.0% | 28.5 | 100.0% | 24.8 | 0.8 X | 43.8 | 0.7 |
| 44788_Exp101_MvdB_LPS10ngml_TA1um_A87 | 84.1% | 60.8 | 49.1% | 98.9% | 0.1% | 235 bp | 92.0% | 100.0% | 59.5 | 100.0% | 54.0 | 1.5 X | 76.6 | 1.8 |
| 44789_Exp101_MvdB_PMA_50ngml_A90 | 82.8% | 95.6 | 49.1% | 98.9% | 0.1% | 231 bp | 91.1% | 100.0% | 93.7 | 100.0% | 85.1 | 2.3 X | 121.2 | 2.4 |
| 44790_Exp101_MvdB_PMA50ngml_TA1um_A91 | 84.7% | 9.8 | 50.1% | 95.8% | 0.2% | 233 bp | 94.5% | 100.0% | 8.2 | 100.0% | 7.4 | 0.2 X | 10.7 | 0.1 |
| 45611_Exp207_MvdB_A_MedCtrl_DMSO_EtOH_A76 | 33.1% | 44.8 | 51.8% | 98.9% | 0.1% | 219 bp | 39.2% | 100.0% | 43.7 | 100.0% | 38.7 | 1.2 X | 60.6 | 0.9 |
| 45612_Exp207_MvdB_B_uMTA_EthOH_A77 | 40.5% | 51.2 | 51.3% | 99.1% | 0.1% | 204 bp | 47.2% | 100.0% | 50.2 | 100.0% | 44.9 | 1.3 X | 67.3 | 1.1 |
| 45613_Exp307_FvdC_Corsk_OH_A78 | 37.4% | 43.5 | 50.4% | 99.1% | 0.1% | 212 bp | 43.8% | 100.0% | 42.7 | 100.0% | 38.6 | 1.1 X | 55.5 | 0.9 |
| 45614_Exp407_MvdD_Dorsk_1umOH_A79 | 33.9% | 39.3 | 51.0% | 98.8% | 0.1% | 204 bp | 39.9% | 100.0% | 38.5 | 100.0% | 34.7 | 1.0 X | 50.0 | 0.8 |
| 45615_Exp207_MvdB_1_4hr_stim_4hr_DMSO_A80 | 38.8% | 38.7 | 51.8% | 98.9% | 0.1% | 218 bp | 45.7% | 100.0% | 38.0 | 100.0% | 33.8 | 1.0 X | 52.2 | 0.7 |
| 45616_Exp207_MvdB_2_4hr_stim_4hr_1umTA_A82 | 34.8% | 47.3 | 52.0% | 99.1% | 0.1% | 212 bp | 41.2% | 100.0% | 46.5 | 100.0% | 41.5 | 1.2 X | 61.6 | 1.0 |
| 45617_Exp207_MvdB_3_28hr_after24hr_4hr_DMSO_A83 | 51.8% | 45.9 | 52.5% | 99.0% | 0.1% | 189 bp | 59.4% | 100.0% | 45.1 | 100.0% | 40.5 | 1.1 X | 58.7 | 1.1 |
| 45618_Exp207_MvdB_4_28hr_after24hr_4hr_1uMTA_A90 | 58.3% | 55.0 | 51.5% | 99.1% | 0.1% | 220 bp | 68.2% | 100.0% | 54.0 | 100.0% | 49.0 | 1.3 X | 68.6 | 1.5 |
| 45619_Exp207_MvdB_5_76hr_after72hr_4hr_DMSO_A91 | 43.2% | 33.2 | 49.5% | 98.8% | 0.1% | 210 bp | 55.2% | 100.0% | 32.4 | 100.0% | 29.5 | 0.8 X | 41.5 | 0.6 |
| 45620_Exp207_MvdB_6_76hr_after72hr_4hr_1uMTA_A92 | 47.6% | 64.4 | 51.7% | 99.2% | 0.1% | 228 bp | 60.7% | 100.0% | 63.4 | 100.0% | 57.8 | 1.6 X | 81.7 | 1.4 |
| 45621_Exp207_MvdB_7_76hr_norest_76hr_DMSO_A73 | 24.0% | 51.1 | 50.6% | 98.9% | 0.1% | 241 bp | 29.8% | 100.0% | 50.3 | 100.0% | 46.4 | 1.2 X | 61.5 | 1.1 |
| 45622_Exp207_MvdB_8_76hr_norest_76hr_1uMTA_A74 | 36.6% | 70.1 | 50.9% | 98.6% | 0.1% | 225 bp | 44.5% | 100.0% | 69.0 | 100.0% | 63.1 | 1.6 X | 83.0 | 1.8 |
| 46164_Exp222_MvdB_RNA_1_medium_PBS_DMSO_PBS_A43 | 36.3% | 18.9 | 56.2% | 98.4% | 0.1% | 215 bp | 50.2% | 100.0% | 18.6 | 100.0% | 8.5 | 1.5 X | 76.9 | 0.3 |
| 46165_Exp222_MvdB_RNA_2_medium_PBS_TA1uM_PBS_A44 | 11.3% | 15.6 | 49.8% | 99.2% | 0.1% | 223 bp | 16.0% | 100.0% | 15.4 | 100.0% | 14.3 | 0.3 X | 18.3 | 0.3 |
| 46166_Exp222_MvdB_RNA_3_medium_PBS_LPS10ngml_DMSO_A45 | 33.8% | 62.6 | 48.2% | 99.3% | 0.1% | 225 bp | 38.2% | 100.0% | 61.7 | 100.0% | 57.8 | 1.4 X | 73.2 | 1.1 |
| 46167_Exp222_MvdB_RNA_4_medium_PBS_TA1uM__LPS10ngml_A62 | 13.6% | 21.5 | 47.4% | 99.3% | 0.1% | 231 bp | 19.1% | 100.0% | 21.2 | 100.0% | 19.9 | 0.5 X | 24.9 | 0.4 |
| 46168_Exp222_MvdB_RNA_5_medium_1ugmlBGluc__DMSO_A63 | 13.2% | 18.6 | 47.8% | 99.0% | 0.1% | 225 bp | 18.5% | 100.0% | 18.3 | 100.0% | 17.1 | 0.4 X | 21.2 | 0.4 |
| 46169_Exp222_MvdB_RNA_6_medium_1ugmlBGluc_TA1uM__PBS_A78 | 13.7% | 17.3 | 48.8% | 98.9% | 0.1% | 242 bp | 19.4% | 100.0% | 17.1 | 100.0% | 15.7 | 0.4 X | 21.6 | 0.4 |
| 46170_Exp222_MvdB_RNA_7_medium_1ugmlBGluc_LPS10ngml__DMSO_A79 | 12.0% | 18.8 | 47.7% | 98.9% | 0.1% | 220 bp | 16.8% | 100.0% | 18.5 | 100.0% | 17.3 | 0.4 X | 21.7 | 0.3 |
| 46171_Exp222_MvdB_RNA_8_medium_1ugmlBGluc_TA1uM__LPS10ngml_A75 | 15.4% | 16.6 | 46.5% | 99.2% | 0.1% | 224 bp | 21.2% | 100.0% | 16.4 | 100.0% | 15.5 | 0.4 X | 18.6 | 0.3 |
Workflow explanation
Assembly stats
fastp
fastp An ultra-fast all-in-one FASTQ preprocessor (QC, adapters, trimming, filtering, splitting...).DOI: 10.1093/bioinformatics/bty560.
Filtered Reads
Filtering statistics of sampled reads.
Insert Sizes
Insert size estimation of sampled reads.
Sequence Quality
Average sequencing quality over each base of all reads.
GC Content
Average GC content over each base of all reads.
N content
Average N content over each base of all reads.
Picard
Picard is a set of Java command line tools for manipulating high-throughput sequencing data.
Insert Size
Plot shows the number of reads at a given insert size. Reads with different orientations are summed.
Mark Duplicates
Number of reads, categorised by duplication state. Pair counts are doubled - see help text for details.
The table in the Picard metrics file contains some columns referring read pairs and some referring to single reads.
To make the numbers in this plot sum correctly, values referring to pairs are doubled according to the scheme below:
READS_IN_DUPLICATE_PAIRS = 2 * READ_PAIR_DUPLICATESREADS_IN_UNIQUE_PAIRS = 2 * (READ_PAIRS_EXAMINED - READ_PAIR_DUPLICATES)READS_IN_UNIQUE_UNPAIRED = UNPAIRED_READS_EXAMINED - UNPAIRED_READ_DUPLICATESREADS_IN_DUPLICATE_PAIRS_OPTICAL = 2 * READ_PAIR_OPTICAL_DUPLICATESREADS_IN_DUPLICATE_PAIRS_NONOPTICAL = READS_IN_DUPLICATE_PAIRS - READS_IN_DUPLICATE_PAIRS_OPTICALREADS_IN_DUPLICATE_UNPAIRED = UNPAIRED_READ_DUPLICATESREADS_UNMAPPED = UNMAPPED_READS
SamTools pre-sieve
Samtools is a suite of programs for interacting with high-throughput sequencing data.DOI: 10.1093/bioinformatics/btp352.
The pre-sieve statistics are quality metrics measured before applying (optional) minimum mapping quality, blacklist removal, mitochondrial read removal, read length filtering, and tn5 shift.Percent Mapped
Alignment metrics from samtools stats; mapped vs. unmapped reads.
For a set of samples that have come from the same multiplexed library, similar numbers of reads for each sample are expected. Large differences in numbers might indicate issues during the library preparation process. Whilst large differences in read numbers may be controlled for in downstream processings (e.g. read count normalisation), you may wish to consider whether the read depths achieved have fallen below recommended levels depending on the applications.
Low alignment rates could indicate contamination of samples (e.g. adapter sequences), low sequencing quality or other artefacts. These can be further investigated in the sequence level QC (e.g. from FastQC).
Alignment metrics
This module parses the output from samtools stats. All numbers in millions.
SamTools post-sieve
Samtools is a suite of programs for interacting with high-throughput sequencing data.DOI: 10.1093/bioinformatics/btp352.
The post-sieve statistics are quality metrics measured after applying (optional) minimum mapping quality, blacklist removal, mitochondrial read removal, and tn5 shift.Percent Mapped
Alignment metrics from samtools stats; mapped vs. unmapped reads.
For a set of samples that have come from the same multiplexed library, similar numbers of reads for each sample are expected. Large differences in numbers might indicate issues during the library preparation process. Whilst large differences in read numbers may be controlled for in downstream processings (e.g. read count normalisation), you may wish to consider whether the read depths achieved have fallen below recommended levels depending on the applications.
Low alignment rates could indicate contamination of samples (e.g. adapter sequences), low sequencing quality or other artefacts. These can be further investigated in the sequence level QC (e.g. from FastQC).
Alignment metrics
This module parses the output from samtools stats. All numbers in millions.
deepTools
deepTools is a suite of tools to process and analyze deep sequencing data.DOI: 10.1093/nar/gkw257.
PCA plot
PCA plot with the top two principal components calculated based on genome-wide distribution of sequence reads
Fingerprint plot
Signal fingerprint according to plotFingerprint
deepTools - Spearman correlation heatmap of reads in bins across the genome
Spearman correlation plot generated by deeptools. Spearman correlation is a non-parametric (distribution-free) method, and assesses the monotonicity of the relationship.
deepTools - Pearson correlation heatmap of reads in bins across the genome
Pearson correlation plot generated by deeptools. Pearson correlation is a parametric (lots of assumptions, e.g. normality and homoscedasticity) method, and assesses the linearity of the relationship.
Samples & Config
| sample | descriptive_name | assembly |
|---|---|---|
| 18419_CL_RNA1_PBMC_minusTA_A41 | PBMC1 | hg38 |
| 18418_CL_RNA2_PBMC_plusTA_A42 | PBMC1_TA4h | hg38 |
| 18417_CL_RNA3_P1_minusTA_A43 | OA_P1_day1 | hg38 |
| 18416_CL_RNA4_P1_plusTA_A44 | OA_P1_day1_TA4h | hg38 |
| 18415_CL_RNA5_P2_minusTA_A45 | OA_P2_day1 | hg38 |
| 18414_CL_RNA6_P2_plusTA_A46 | OA_P2_day1_TA4h | hg38 |
| 18413_CL_RNA7_P3_minusTA_A47 | OA_P3_day1 | hg38 |
| 18412_CL_RNA8_P3_plusTA_A48 | OA_P3_day1_TA4h | hg38 |
| 18411_CL_RNA9_P4_minusTA_A49 | OA_P4_day1 | hg38 |
| 18410_CL_RNA10_P4_plusTA_A50 | OA_P4_day1_TA4h | hg38 |
| 18409_CL_RNA11_P5_minusTA_A51 | OA_P5_day1 | hg38 |
| 18408_CL_RNA12_P5_plusTA_A52 | OA_P5_day1_TA4h | hg38 |
| 44115_Exp188_MvdB_RNA_1_DMSO_A10 | PMBC2 | hg38 |
| 44116_Exp188_MvdB_RNA_2_TA_1um_A11 | PMBC2_TA4h | hg38 |
| 44117_Exp188_MvdB_RNA_3_LPS_10ngml_A12 | PMBC2_LPS4h | hg38 |
| 44118_Exp188_MvdB_RNA_4_LPSTA_A14 | PMBC2_TA_LPS4h | hg38 |
| 44119_Exp188_MvdB_RNA_5_4h_ctrl_A20 | OA_P6 | hg38 |
| 44120_Exp188_MvdB_RNA_6_4h_triam_A23 | OA_P6_TA4h | hg38 |
| 44121_Exp188_MvdB_RNA_7_4h_LPS_A24 | OA_P6_LPS4h | hg38 |
| 44122_Exp188_MvdB_RNA_8_4h_triam__LPS_A25 | OA_P6_TA_LPS4h | hg38 |
| 44123_Exp188_MvdB_RNA_9_3d_Ctrl_A27 | OA_P6_day3 | hg38 |
| 44124_Exp188_MvdB_RNA_10_3d_triam_A28 | OA_P6_day3_TA72h | hg38 |
| 44125_Exp188_MvdB_RNA_11_5d_Ctrl_A29 | OA_P6_day5 | hg38 |
| 44126_Exp188_MvdB_RNA_12_5d_triam_A30 | OA_P6_day5_TA124h | hg38 |
| 44781_Exp101_MvdB_Medium_A79 | OA_P7 | hg38 |
| 44785_Exp101_MvdB_TA_1um_A83 | OA_P7_TA4h | hg38 |
| 44784_Exp101_MvdB_LPC_10ngml_A82 | OA_P7_LPS4h | hg38 |
| 44788_Exp101_MvdB_LPS10ngml_TA1um_A87 | OA_P7_TA_LPS4h | hg38 |
| 44783_Exp101_MvdB_Ionomycine_149ngml_A81 | OA_P7_Iono4h | hg38 |
| 44787_Exp101_MvdB_Ionomycine149ngml_TA1um_A26 | OA_P7_TA_Iono4h | hg38 |
| 44782_Exp101_MvdB_PMA_10ngml_A80 | OA_P7_PMA10_4h | hg38 |
| 44786_Exp101_MvdB_PMA10ngml_TA1um_A84 | OA_P7_TA_PMA10_4h | hg38 |
| 44789_Exp101_MvdB_PMA_50ngml_A90 | OA_P7_PMA50_4h | hg38 |
| 44790_Exp101_MvdB_PMA50ngml_TA1um_A91 | OA_P7_TA_PMA50_4h | hg38 |
| 45611_Exp207_MvdB_A_MedCtrl_DMSO_EtOH_A76 | OA_P8 | hg38 |
| 45612_Exp207_MvdB_B_uMTA_EthOH_A77 | OA_P8_TA4h | hg38 |
| 45613_Exp307_FvdC_Corsk_OH_A78 | OA_P8_forsk4h | hg38 |
| 45614_Exp407_MvdD_Dorsk_1umOH_A79 | OA_P8_TA_forsk4h | hg38 |
| 45615_Exp207_MvdB_1_4hr_stim_4hr_DMSO_A80 | OA_P8_4h | hg38 |
| 45616_Exp207_MvdB_2_4hr_stim_4hr_1umTA_A82 | OA_P8_4h_TA4h | hg38 |
| 45617_Exp207_MvdB_3_28hr_after24hr_4hr_DMSO_A83 | OA_P8_24h | hg38 |
| 45618_Exp207_MvdB_4_28hr_after24hr_4hr_1uMTA_A90 | OA_P8_24h_TA4h | hg38 |
| 45619_Exp207_MvdB_5_76hr_after72hr_4hr_DMSO_A91 | OA_P8_72h | hg38 |
| 45620_Exp207_MvdB_6_76hr_after72hr_4hr_1uMTA_A92 | OA_P8_72h_TA4h | hg38 |
| 45621_Exp207_MvdB_7_76hr_norest_76hr_DMSO_A73 | OA_P8_76h | hg38 |
| 45622_Exp207_MvdB_8_76hr_norest_76hr_1uMTA_A74 | OA_P8_TA76h | hg38 |
| 46164_Exp222_MvdB_RNA_1_medium_PBS_DMSO_PBS_A43 | OA_P9_120h | hg38 |
| 46165_Exp222_MvdB_RNA_2_medium_PBS_TA1uM_PBS_A44 | OA_P9_120h_TA4h | hg38 |
| 46166_Exp222_MvdB_RNA_3_medium_PBS_LPS10ngml_DMSO_A45 | OA_P9_120h_LPS4h | hg38 |
| 46167_Exp222_MvdB_RNA_4_medium_PBS_TA1uM__LPS10ngml_A62 | OA_P9_120h_TALPS4h | hg38 |
| 46168_Exp222_MvdB_RNA_5_medium_1ugmlBGluc__DMSO_A63 | OA_P9_120hBG | hg38 |
| 46169_Exp222_MvdB_RNA_6_medium_1ugmlBGluc_TA1uM__PBS_A78 | OA_P9_120hBG_TA4h | hg38 |
| 46170_Exp222_MvdB_RNA_7_medium_1ugmlBGluc_LPS10ngml__DMSO_A79 | OA_P9_120hBG_LPS4h | hg38 |
| 46171_Exp222_MvdB_RNA_8_medium_1ugmlBGluc_TA1uM__LPS10ngml_A75 | OA_P9_120hBG_TALPS4h | hg38 |
# tab-separated file of the samples
samples: samples.tsv
# pipeline file locations
result_dir: ./results_new # where to store results
genome_dir: ./genomes # where to look for or download the genomes
fastq_dir: ./fastqs
# contact info for multiqc report and trackhub
email: slrinzema@science.ru.nl
create_trackhub: true
# how to handle replicates
technical_replicates: merge # change to "keep" to not combine them
# which trimmer to use
trimmer: fastp
# which quantifier to use
quantifier: htseq # or salmon or featurecounts
# which aligner to use (not used for the gene counts matrix if the quantifier is Salmon)
aligner: star
bam_sorter:
samtools:
coordinate
# filtering after alignment (not used for the gene counts matrix if the quantifier is Salmon)
remove_blacklist: true
min_mapping_quality: 255 # (only keep uniquely mapped reads from STAR alignments)
only_primary_align: true
remove_dups: false # keep duplicates (check dupRadar in the MultiQC)
# differential gene expression analysis
# for explanation, see: https://vanheeringen-lab.github.io/seq2science/content/DESeq2.html
#contrasts:
# - 'stage_2_1'