
View Run Metrics
When run metrics are available, Sequencing Analysis Viewer (SAV) opens automatically and displays them.
Metrics appear in the form of plots, graphs, and tables. For more information, see the
Sequencing Analysis
Viewer User Guide (document # 15020619)
.
1
To view updated metrics, select Refresh at any time during the run.
Prepare Reagents for Read 2
Before the completion of Read 1 and any index reads, prepare reagents for Read 2 resynthesis and fresh ICB
for Read 2. Load reagents when prompted by the control software.
Prepare Paired-End Reagents
Paired-end reagents are used during the Read 2 resynthesis step of a paired-end sequencing run.
NOTE
Nextera libraries require HP11, a sequencing primer provided in the TruSeq Dual Index Sequencing Primer
Box. All other libraries use HP7.
Thaw Paired-End Reagents
1
Remove the following reagents from -25°C to -15°C storage:
u
For non-indexed or single-indexed runs—AMX2, APM2, AT2, BMX, HP3, HP7 or HP11, HT2, LMX2,
and RMR
u
For dual-indexed runs—AMX2, APM2, AT2, BMX, HP3, HP7 or HP11, HT2, and LMX2
u
For paired-end runs—HP3
2
Thaw reagents in a beaker filled with room temperature deionized water for about 20 minutes.
3
Set aside AMX2, BMX, LMX2, and RMR on ice.
Prepare AMX2, APM2, AT2, BMX, HP3, HP7, HP11, HT2, and LMX2
1
Invert each tube to mix.
2
Centrifuge at 1000 rpm for 1 minute.
3
Set aside AMX2, BMX, and LMX2 on ice.
4
Set aside APM2, AT2, HP3, HP7, HP11, and HT2 at room temperature.
Prepare HP3 for Paired-End Runs
1
Invert to mix, and then pulse centrifuge.
2
Transfer 2.85 ml PW1 to an empty 15 ml conical tube, and then add 150 µl HP3.
3
Invert to mix.
4
Centrifuge at 1000 rpm for 1 minute.
5
Set aside at room temperature.
Document # 15011190 v03
For Research Use Only. Not for use in diagnostic procedures.
40
HiSeq 2000 System Guide